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| Product | Description | |
|---|---|---|
| 2,6-Diisopropylnaphthalene | 2, 6-Diisopropyl naphthalene. Group: Biochemicals. Alternative Names: 2, 6-Bis (1-methylethyl) naphthalene; NSC 166467. Grades: Highly Purified. CAS No. 24157-81-1. Pack Sizes: 1g. Molecular Formula: C16H20, Molecular Weight: 212.33. US Biological Life Sciences. |  Worldwide |
| 2,6-Diisopropylnaphthalene | 2,6-Diisopropylnaphthalene. Group: Pressure & heat sensitive recording materials heat & pressure sensitive dyes. CAS No. 24157-81-1. Product ID: 2,6-di(propan-2-yl)naphthalene. Molecular formula: 212.33g/mol. Mole weight: C16H20. CC(C)C1=CC2=C(C=C1)C=C(C=C2)C(C)C. InChI=1S/C16H20/c1-11 (2)13-5-7-16-10-14 (12 (3)4)6-8-15 (16)9-13/h5-12H, 1-4H3. GWLLTEXUIOFAFE-UHFFFAOYSA-N. |  |
| Diisopropylnaphthalene (mixture of isomers) | Diisopropylnaphthalene (mixture of isomers). Uses: For analytical and research use. Group: Pesticides & metabolites; pesticides & metabolites. CAS No. 38640-62-9. IUPAC Name: 1,5-di(propan-2-yl)naphthalene. Molecular Formula: C16H20. Mole Weight: 212.33. Catalog: APS38640629. SMILES: CC(C)c1cccc2c(cccc12)C(C)C. Format: Neat. Shipping: Room Temperature. |  |
| Sodium diisopropylnaphthalenesulphonate | Use as penetrating agent, wetting agent. Use as emulsifying agent, dispersing agent. Use as hydrotrope. Group: Anionic surfactants. Alternative Names: Sodium bis(1-methylethyl)naphthalenesulfonate. CAS No. 1322-93-6. Molecular formula: C16H19NaO3S. Mole weight: 314.38. Catalog: ACM1322936. |  |
| (+)-Apogossypol | (+)-Apogossypol is a potent inhibitor of Bcl-2 family proteins, binding and inhibiting Bcl-2 and Bcl-X(L) with high affinity and induces apoptosis of tumor cell lines. Uses: A potent inhibitor of bcl-2 family proteins. Synonyms: (R)-5,5'-diisopropyl-3,3'-dimethyl-[2,2'-binaphthalene]-1,1',6,6',7,7'-hexaol; methanol;3-methyl-5-propan-2-yl-2-(1,6,7-trihydroxy-3-methyl-5-propan-2-ylnaphthalen-2-yl)naphthalene-1,6,7-triol; Apogossypol. Grades: ≥95%. CAS No. 66389-74-0. Molecular formula: C29H34O7. Mole weight: 494.58. |  |
| Bedaquiline Impurity 2 | Bedaquiline Impurity 2. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (1R,2S)-1-(6-(diisopropylamino)-2-methoxyquinolin-3-yl)-4-(dimethylamino)-2-(naphthalen-1-yl)-1-phenylbutan-2-ol. Molecular Formula: C38H45N3O2. Mole Weight: 575.78. Catalog: APB03666. | |
| (R)-3, 3'-Bis(3, 5-diisopropylphenyl)-[1, 1'-binapthalene]-2, 2'-diol | (R)-3, 3'-Bis(3, 5-diisopropylphenyl)-[1, 1'-binapthalene]-2, 2'-diol, also known as (R)-BINAP, is an important chiral ligand used in asymmetric synthesis of organic compounds. It is a widely used compound in chemical and pharmaceutical industries due to its ability to catalyze a variety of reactions with high enantioselectivity. This review will discuss the synthesis of (R)-BINAP, its scientific research applications, its mechanism of action, its biochemical and physiological effects, the advantages and limitations for lab experiments, and the potential future directions of research. Uses: (r)-binap is widely used in asymmetric synthesis of various organic compounds, including chiral drugs, natural products, and polymers. it is particularly useful in the synthesis of polycyclic compounds and chiral alcohols, and has been used in the synthesis of a variety of drugs, including the antimalarial drug artemisinin, the anti-cancer drug paclitaxel, and the anti-hiv drug tenofovir. in addit. Group: Chiral binol ligands. CAS No. 1435948-31-4. Molecular formula: C44H46O2. Mole weight: 606.8 g/mol. IUPACName: 3-[3,5-di(propan-2-yl)phenyl]-1-[3-[3,5-di(propan-2-yl)phenyl]-2-hydroxynaphthalen-1-yl]naphthalen-2-ol. Canonical SMILES: CC (C)C1=CC (=CC (=C1)C2=CC3=CC=CC=C3C (=C2O)C4=C (C (=CC5=CC=CC=C54)C6=CC (=CC (=C6)C (C)C)C (C)C)O)C (C)C. Catalog: ACM1435948314-1. | |
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