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Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a K i of 2.93 nM and exhibits an IC 95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture [1]. Uses: Scientific research. Group: Natural products. Alternative Names: DMP 266; EFV; L-743726. CAS No. 154598-52-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-10572.
Efavirenz 1-Desamine
Efavirenz 1-Desamine is an analog of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Alternative Names: 7-Chloro-1- (cyclopropylethynyl) -1- (trifluoromethyl) isochroman-3-one. Grades: Highly Purified. Pack Sizes: 500ug, 1mg, 2.5mg. Molecular Formula: C15H10ClF3O2. US Biological Life Sciences.
Worldwide
Efavirenz Benzoylaminoalcohol Impurity
An impurity arising in the synthesis of Efavirenz. Synonyms: rac N-[4-Chloro-2-[3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propynyl]phenyl]-4-methoxybenzamide. Grades: > 95%. CAS No. 1189491-03-9. Molecular formula: C21H17ClF3NO3. Mole weight: 423.81.
Efavirenz impurity (6-chloro-4-[2-(2-methylcyclopropyl)ethynyl]-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one) is an impurity of Efavirenz, a medication used to treat HIV/AIDS. Grades: > 95%. CAS No. 1217623-65-8. Molecular formula: C15H11ClF3NO2. Mole weight: 329.71.
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsimpurity standardspharmaceutical toxicology. Alternative Names: Efavirenz Racemic, ((+/-)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one).
Efavirenz Ready Made Solution
10 mg/mL in DMSO. Group: Fluorescence/luminescence spectroscopy.
Efavirenz Related Compound A
Cas No. 209414-27-7.
Efavirenz Related Compound A
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Efavirenz Related Compound B
Efavirenz impurity. Synonyms: (4S)-6-Chloro-4-[(1E)-2-cyclopropylethenyl]-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-Benzoxazin-2-one; USP Efavirenz Related Compound B. Grades: > 95%. CAS No. 440124-96-9. Molecular formula: C14H11ClF3NO2. Mole weight: 317.69.
Efavirenz Related Compound B
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Efavirenz Related Compound C
An impurity of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor and antiviral agent. Synonyms: 2-Cyclopropyl-6-chloro-4-(trifluoromethyl)quinoline, USP Efavirenz Related Compound C. Grades: > 95%. CAS No. 391860-73-4. Molecular formula: C13H9ClF3N. Mole weight: 271.67.
Efavirenz Related Compound C
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Efavirenz (Sustiva, MDP-266, L-743726)
A nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: (4S)-6-Chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; DMP 266; L 743726; Stocrin; Sustiva. Grades: Highly Purified. CAS No. 154598-52-4. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C14H9ClF3NO2, Molecular Weight: 315.67. US Biological Life Sciences.
Worldwide
2-Deoxo-3-desoxy Efavirenz
2-Deoxo-3-desoxy Efavirenz is a derivative of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C15H13ClF3N, Molecular Weight: 299.72. US Biological Life Sciences.
Worldwide
8-Hydroxy Efavirenz
8-Hydroxy Efavirenz is a metabolite of Efavirenz. Synonyms: (4S)-6-Chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; 8-Hydroxyefavirenz. Grades: > 95%. CAS No. 205754-33-2. Molecular formula: C14H9ClF3NO3. Mole weight: 331.67.
(E)-Dihydro Efavirenz is an impurity of the nonnucleoside HIV-1 reverse transcriptase inhibitor Efavirenz. Group: Biochemicals. Alternative Names: (4S)-6-Chloro-4-[(1E)-2-cyclopropylethenyl]-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-Benzoxazin-2-one; SR 695. Grades: Highly Purified. CAS No. 440124-96-9. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
(E)-Dihydro Efavirenz
(E)-Dihydro Efavirenz. Uses: For analytical and research use. Group: Impurity standards. CAS No. 440124-96-9. Pack Sizes: 5MG. IUPAC Name: (4S)-6-chloro-4-[(E)-2-cyclopropylethenyl]-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one. Molecular formula: C14H11ClF3NO2. Mole weight: 317.69. Catalog: APS440124969. SMILES: FC(F)(F)[C@]1(OC(=O)Nc2ccc(Cl)cc12)\C=C\C3CC3. Format: Neat. Shipping: Room Temperature.
ent-Efavirenz
A nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Alternative Names: (4R)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; (R)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; L 743725. Grades: Highly Purified. CAS No. 154801-74-8. Pack Sizes: 2.5mg. US Biological Life Sciences.
Worldwide
Ent efavirenz
Ent efavirenz. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (4R)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; (R)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro -4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; L 743725. Product Category: Heterocyclic Organic Compound. Appearance: Off-White to Pale Yellow Solid. CAS No. 154801-74-8. Molecular formula: C14H9ClF3NO2. Mole weight: 315.67. Purity: 0.96. IUPACName: (4R)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one. Density: 1.53g/cm³. Product ID: ACM154801748. Alfa Chemistry ISO 9001:2015 Certified.
rac 7-Hydroxy Efavirenz
A metabolite of Efavirenz (minor). Group: Biochemicals. Alternative Names: 6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-7-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one. Grades: Highly Purified. CAS No. 205754-50-3. Pack Sizes: 500ug, 1mg, 2mg. US Biological Life Sciences.
Worldwide
rac 7-Hydroxy Efavirenz-d4 (Major)
An isotope labeled metabolite of Efavirenz (minor). A representative lot was 84% d4, 12% d5, 2% d3 and 1% d6. Group: Biochemicals. Alternative Names: 6-Chloro-4-(cyclopropyl-d4-ethynyl)-1,4-dihydro-7-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
rac 8,14-Dihydroxy Efavirenz
A metabolite of Efavirenz (secondary metabolism. Group: Biochemicals. Alternative Names: 6-Chloro-1, 4-dihydro-8-hydroxy-4-[ (1-hydroxycyclopropyl) ethynyl]-4- (trifluoromethyl) -2H-3, 1-benzoxazin-2-one. Grades: Highly Purified. CAS No. 1189909-96-3. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
rac 8,14-Dihydroxy Efavirenz-d4
A labeled metabolite of Efavirenz (secondary metabolism. Group: Biochemicals. Alternative Names: 6-Chloro-1,4-dihydro-8-hydroxy-4-[(1-hydroxycyclopropyl-d4)ethynyl]-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one. Grades: Highly Purified. CAS No. 1189859-26-4. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
rac 8-Hydroxy Efavirenz
A metabolite of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
rac 8-Hydroxy Efavirenz
A metabolite of Efavirenz , a nonnucleoside HIV-1 reverse transcriptase inhibitor. Synonyms: 6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one. Grades: > 95%. CAS No. 205754-32-1. Molecular formula: C14H9ClF3NO3. Mole weight: 331.68.
rac 8-Hydroxy Efavirenz-d4
A labellebed metabolite of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
Worldwide
rac Efavirenz
rac Efavirenz is a mixture of both enantiomers for Efavirenz. Synonyms: 6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one. Grades: > 95%. CAS No. 177530-93-7. Molecular formula: C14H9ClF3NO2. Mole weight: 315.67.
rac Efavirenz-d4
Labelled Efavirenz (E42500). A nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: 6-Chloro-4-(2-cyclopropyl-d4-ethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; DMP 266-d4; L 743726-d4; Stocrin-d4; Sustiva-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
rac Efavirenz-d5 (major)
Labeled Efavirenz. A nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Alternative Names: 6-Chloro-4-(2-cyclopropyl-d5-ethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; DMP 266-d5; L 743726-d5. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
1- (2- ( (tert-Butyldimethylsilyl) oxy) -5-chlorophenyl) -2, 2, 2-trifluoroethanone is an intermediate in the synthesis of Efavirenz De(1-amino-3-oxo)-1-oxo-3-amine, which is an analog of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg, 500mg. Molecular Formula: C14H18ClF3O2Si. US Biological Life Sciences.
Worldwide
1,3-Bis(methoxymethyl)-2-nitrobenzene
1,3-Bis(methoxymethyl)-2-nitrobenzene is an intermediate in the synthesis of 2,6-Dihydroxymethyl Rilpivirine (D446615), which is an analog of Rilpivirine (R509800) a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg. Molecular Formula: C10H13NO4. US Biological Life Sciences.
Worldwide
(1Z)-Rilpivirine
(1Z)-Rilpivirine is a stereoisomer of Rilpivirine (R509800) which is a non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. Group: Biochemicals. Grades: Highly Purified. CAS No. 500287-94-5. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C22H18N6, Molecular Weight: 366.42. US Biological Life Sciences.
2- (2- (2- ( (tert-Butyldimethylsilyl) oxy) ethyl) -5-chlorophenyl) -4-cyclopropyl-1, 1, 1-trifluorobut-3-yn-2-ol is an analog of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C21H28ClF3O2Si. US Biological Life Sciences.
Worldwide
2,2,2-Trifluoroethanol-1,1-d2
Isotope labelled 2,2,2-Trifluoroethanol (T790175), is used in the synthesis of competitive inhibitors for phospholipase A2. Used in the preparation of a key Efavirenz (E425000) intermediate, a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 132248-58-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C2HD2F3O, Molecular Weight: 102.05. US Biological Life Sciences.
2-(5-Chloro-2-(2-hydroxyethyl)phenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol is an analog of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C15H14ClF3O2. US Biological Life Sciences.
2- (5-Chloro-2- (4-methoxybenzamido) phenyl) -4-cyclopropyl-1, 1, 1-trifluorobut-3-yn-2-yl 4-Methoxybenzoate is an impurity of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
2, 6-Bis (methoxymethyl)aniline
2, 6-Bis (methoxymethyl)aniline is an intermediate in the synthesis of 2,6-Dihydroxymethyl Rilpivirine (D446615), which is an analog of Rilpivirine (R509800) a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C10H15NO2. US Biological Life Sciences.
2-Amino-5-chloro-α - (cyclopropylethynyl) -α - (trifluoromethyl) benzenemethanol-d4 is an isotope labelled impurity of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C13H7D4ClF3NO. US Biological Life Sciences.
Worldwide
2-Hydroxymethyl Rilpivirine
2-Hydroxymethyl Rilpivirine is an analog of Rilpivirine (R509800) a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 1798429-64-7. Pack Sizes: 500ug, 5mg. Molecular Formula: C22H18N6O. US Biological Life Sciences.
Worldwide
2-Nitro-1,3-benzenedimethanol
2-Nitro-1,3-benzenedimethanol is an intermediate in the synthesis of 2,6-Dihydroxymethyl Rilpivirine (D446615), which is an analog of Rilpivirine (R509800) a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 16578-60-2. Pack Sizes: 50mg, 100mg. Molecular Formula: C8H9NO4. US Biological Life Sciences.
(2S, 3R, 4R, 5S) -6- ( (2- ( (2- ( (4-Cyanophenyl) amino) pyrimidin-4-yl) amino) -5- ( (E) -2-cyanovinyl) -3- (hydroxymethyl) benzyl) oxy) -3, 4, 5-trihydroxytetrahydro-2H-pyran-2-carboxylic Acid is a metabolite of Rilpivirine (R509800), which is a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine is an anti-HIV agent that seems to be well tolerated with less CNS disturbance than Efavirenz and has non-teratogenic potential. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C28H26N6O8, Molecular Weight: 574.54. US Biological Life Sciences.
(2S, 3R, 4R, 5S) -6- ( (2- ( (2- ( (4-Cyanophenyl) amino) pyrimidin-4-yl) amino) -5- ( (E) -2-cyanovinyl) -3-methylbenzyl) oxy) -3, 4, 5-trihydroxytetrahydro-2H-pyran-2-carboxylic Acid is a metabolite of Rilpivirine (R509800), which is a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine is an anti-HIV agent that seems to be well tolerated with less CNS disturbance than Efavirenz and has non-teratogenic potential. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C28H26N6O7, Molecular Weight: 558.54. US Biological Life Sciences.
Worldwide
4-Chloro-2-trifluoroacetylaniline
An intermediate in the synthesis of Efavirenz-d4. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
(4S)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-2-(4-methoxyphenyl)-4-(trifluoromethyl)-2H-3,1-benzoxazine (Mixture of 2 Diastereomers)
An impurity arising in the synthesis of Efavirenz. Group: Biochemicals. Alternative Names: (4S)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-2-(4-methoxyphenyl)-4-(trifluoromethyl)-2H-3,1-benzoxazine. Grades: Highly Purified. CAS No. 209414-26-6. Pack Sizes: 5mg. US Biological Life Sciences.
An intermediate in the synthesis of Efavirenz-d4. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Fosdevirine
Fosdevirine is a highly potent next-generation Anti-HIV nonnucleoside reverse transcriptase inhibitor (NNRTI) with an EC50 of 11 nM. It is a novel and once-daily (QD) inhibitor with activity against efavirenz-resistant strains. It demonstrated potent antiviral activity in treatment-naive HIV-infected subjects, and had favorable PK and resistance profiles. It was originally developed by idenix pharmaceuticals and was in clinical phase 2, but now it has been terminated. Uses: Fosdevirine has potent antiviral activity. Synonyms: GSK2248761; GSK-2248761; GSK 2248761; GSK2248761A; GSK-2248761A; GSK 2248761A; IDX899; IDX-899; IDX 899, Fosdevirine;Methyl (E)-(2-carbamoyl-5-chloro-1H-indol-3-yl)(3-(2-cyanovinyl)-5-methylphenyl)phosphinate;5-Chloro-3-[[3-[(E)-2-cyanoethenyl]-5-methylphenyl]-methoxyphosphoryl]-1H-indole-2-carboxamide. Grades: 95%. CAS No. 1018450-26-4. Molecular formula: C20H17ClN3O3P. Mole weight: 413.80.
IDX899
IDX899 is a novel next-generation nonnucleoside reverse transcriptase inhibitor (NNRTI) with activity against efavirenz-resistant strains. It is used in the treatment of treatment-naive HIV-1-infected subjects. Uses: Idx899 is used in the treatment of treatment-naive hiv-1-infected subjects. Synonyms: GSK 224876 ; GSK-224876 ; GSK224876; IDX-899; IDX 899; IDX899; 5-Chloro-3-[[3-[(E)-2-cyanovinyl]-5-methyl-phenyl]-methoxy-phosphoryl]-1H-indole-2-carboxamide;Methyl (E)-(2-carbamoyl-5-chloro-1H-indol-3-yl)(3-(2-cyanovinyl)-5-methylphenyl)phosphinate;GSK-224876;GSK224876;(R,E)-methyl (2-carbamoyl-5-chloro-1H-indol-3-yl)(3-(2-cyanovinyl)-5-methylphenyl)phosphinate. Grades: 95%. CAS No. 1097733-15-7. Molecular formula: C20H17ClN3O3P. Mole weight: 413.79.
An intermediate in the synthesis of ent Efavirenz. Group: Biochemicals. Alternative Names: 1-[5-Chloro-2-[[ (4-methoxyphenyl) methyl]amino]phenyl]-2, 2, 2-trifluoroethanone. Grades: Highly Purified. CAS No. 173676-54-5. Pack Sizes: 100mg. US Biological Life Sciences.
An intermediate of ent Efavirenz. Group: Biochemicals. Alternative Names: (α R) -Chloro-α - (cyclopropylethynyl) -2-[[ (4-methoxyphenyl) methyl]amino]-α - (trifluoromethyl) benzenemethanol. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Efavirenz impurity. Group: Biochemicals. Alternative Names: (α R) -2-Amino-5-chloro-α - (2-cyclopropylethynyl) -α - (trifluoromethyl) benzenemethanol. Grades: Highly Purified. CAS No. 927812-33-7. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Rilmenidine Impurity B
An impurity of Rilmenidine,Rilmenidine Is A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Synonyms: 1-(2-chloroethyl)-3-(dicyclopropylmethyl)urea. Grades: > 95%. Molecular formula: C10H17ClN2O. Mole weight: 216.71.
Rilmenidine Impurity C
An impurity of Rilmenidine,Rilmenidine Is A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Synonyms: 2-[N-(Dicyclopropylmethyl)imino]-N-(dicyclopropylmethyl)isooxazoline Synonyms: 1,1-Dicyclopropyl-N-(3-(dicyclopropylmethyl)oxazolidin-2-ylidene)methanamine. Grades: > 95%. Molecular formula: C17H26N2O. Mole weight: 274.41.
Rilpivirine
A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Synonyms: R 278474; TMC 278; R-278474; R278474; TMC278; TMC-278. Grades: 0.98. CAS No. 500287-72-9. Molecular formula: C22H18N6. Mole weight: 366.428.
Rilpivirine
A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. Group: Biochemicals. Alternative Names: 4- [ [4- [ [4- [ (1E) -2-Cyanoethenyl] -2, 6-dimethylphenyl] amino] -2-pyrimidinyl] amino] benzonitrile. Grades: Highly Purified. CAS No. 500287-72-9. Pack Sizes: 2.5mg, 5mg, 10mg, 25mg. Molecular Formula: C22H18N6, Molecular Weight: 366.42. US Biological Life Sciences.
An impurity of Rilpivirine. Rilpivirine is a non-nucleoside reverse transcriptase inhibitor.It seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. Rilpivirine is an anti-HIV agent. Synonyms: [4-[[2[(4-Cyanophenyl)amino]pyrimidin-4-yl]amino]-3, 5-Dimethylphenyl]prop-2-Enamid. Grades: > 95%. Molecular formula: C22H20N6O. Mole weight: 384.44.
An impurity of Rilpivirine. Rilpivirine is a non-nucleoside reverse transcriptase inhibitor.It seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. Rilpivirine is an anti-HIV agent. Grades: > 95%. Molecular formula: C22H20N6O. Mole weight: 384.44.
An impurity of Rilmenidine,Rilmenidine Is A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. Synonyms: 4-[(4-Chloro-2-pyrimidinyl)amino] benzonitrile. Grades: > 95%. Molecular formula: C11H7ClN4. Mole weight: 230.66.
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