Allyl Cinnamate Suppliers USA

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Product
Allyl Cinnamate Allyl Cinnamate. Group: Biochemicals. Alternative Names: 3-Phenyl-2-propenoic Acid 2-Propenyl Ester; Cinnamic Acid Allyl ester; Allyl Cinnamate; NSC 20972. Grades: Highly Purified. CAS No. 1866-31-5. Pack Sizes: 50g. Molecular Formula: C10H11NO2, Molecular Weight: 188.22. US Biological Life Sciences. USBiological 3
Worldwide
Cinnamic acid allyl ester Cinnamic acid allyl ester. Group: Monomers. Alternative Names: Wln: 1U2ov1U1r; (E)-cinnamic acid allyl ester; trans-allyl cinnamate; allyl3-phenylacrylate; allyl trans-cinnamate; (E)-allyl cinnamate; propenylcinnamate; prop-2-enyl 3-phenylacrylate; Allyl 3-phenylacrylate; Allyl Cinnamate; FEMA 2022; Cinnamic Acid All. CAS No. 1866-31-5. Product ID: prop-2-enyl (E)-3-phenylprop-2-enoate. Molecular formula: 188.22. Mole weight: C12< / sub>H12< / sub>O2< / sub>. KCMITHMNVLRGJU-CMDGGOBGSA-N. 96%. Alfa Chemistry Materials 7
Cinnamyl acetate Cinnamyl acetate. CAS No. 103-54-8. Pack Sizes: 250 mL in glass bottle. Product ID: CDC10-0194. Molecular formula: C11H12O2. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; Cinnamyl acetate; CDC10-0194; 103-54-8; C11H12O2; 203-121-9; MFCD00008722; 103-54-8. Purity: 0.99. EC Number: 203-121-9. Physical State: Powder. Solubility: alcohol: soluble(lit.). Quality Level: 100. Boiling Point: 265 °C (lit.). Melting Point: 30 °C. Density: 1.057 g/mL at 25 °C. Product Description: Cinnamyl acetate is a fragrance ingredient. Palladium catalyzed allylic alkylation of cinnamyl acetate using sodium diethyl 2-methylmalonate and novel ferrocenyl Schiff base has been investigated. CD Formulation
Naftifine Naftifine is a topical, synthetic, broad spectrum allylamine derivate. It has antifungal, antibacterial and anti-inflammatory activity and is used for the treatment of tinea pedis, tinea cruris, and tinea corporis. It can be fungicidal or fungistatic depending on the concentration and the organisms involved. It appears to interfere with sterol biosynthesis by inhibiting the enzyme squalene 2,3-epoxidase. It was developed by Merz pharma and has been listed. Uses: Naftifine has antifungal, antibacterial and anti-inflammatory activity and is used for the treatment of tinea pedis, tinea cruris, and tinea corporis. Synonyms: Naftifinum; AW105843; AW-105843; SN105843; SN-105843; N-trans-cinnamyl-n-methyl-(1-naphthylmethyl)amine. Grades: 98%. CAS No. 65472-88-0. Molecular formula: C21H21N. Mole weight: 287.41. BOC Sciences 11
Naftifine cis-Isomer An impurity of Naftifine, which is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,5-epoxidase enzyme. Synonyms: (Z)-N-Methyl-N-(3-phenyl-2-propen-1-yl)-1-naphthalenemethanamine Hydrochloride;(Z)-N-Cinnamyl-N-methyl-1-naphthalenemethanamine Hydrochloride. Grades: > 95%. CAS No. 65473-08-7. Molecular formula: C21H21N. Mole weight: 287.41. BOC Sciences 6
(R)-α-(3-phenyl-allyl)-proline hydrochloride Heterocyclic Organic Compound. Alternative Names: (R)-2-Cinnamylpyrrolidine-2-carboxylic acid hydrochloride, 1049739-31-2, KB-209899. CAS No. 1049739-31-2. Molecular formula: C14H18ClNO2. Mole weight: 267.75. Purity: 0.96. IUPACName: (2R)-2-(3-phenylprop-2-enyl)pyrrolidine-2-carboxylic acid;hydrochloride. Canonical SMILES: C1CC(NC1)(CC=CC2=CC=CC=C2)C(=O)O.Cl. Catalog: ACM1049739312. Alfa Chemistry. 5

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