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2-methylcinnamic acid, predominantly trans

2-METHYLCINNAMIC ACID 99% PREDOMINANTL Y TRANS

Catalog No.
C005B-026662
Manufacturer No.
433101-5G
Manufacturer Name
Sigma-Aldrich
Quantity
5
Unit of Measure
GR

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2-Methylcinnamic acid has been reported to exhibit strong anti-fungal activity against white-rot fungus Lenzites betulina and brown-rot fungus Laetiporus sulphureus . Hydrogenation of 2-methylcinnamic acid using Walphos ligands and their

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General description

2-Methylcinnamic acid has been reported to exhibit strong anti-fungal activity against white-rot fungus Lenzites betulina and brown-rot fungus Laetiporus sulphureus. Hydrogenation of 2-methylcinnamic acid using Walphos ligands and their biferrocene analogs has been studied.

Application

2-Methylcinnamic acid may be used as starting reagent for the total synthesis of the cytotoxic alkaloid, 22-hydroxyacuminatine and for the preparation of (E)-2-methylcinnamic acid i-butylammonium salt.

Molecular Weight: 162.19. Empirical Formula: C10H10O2. linearFormula: CH3C6H4CH: CHCO2H. Quality Level: 100. Assay: 99%. mp: 174-176 . °C (lit.). SMILES string: Cc1ccccc1\C: C\C(O): O. InChI: 1S/C10H10O2/c1-8-4-2-3-5-9(8)6-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-6+. InChI key: RSWBWHPZXKLUEX-VOTSOKGWSA-N. Storage Class Code: 11 - Combustible Solids. WGK: WGK 3. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).
UPC:
12352106
Condition:
New
HazmatClass:
No
MPN:
433101-5G
CAS:
2373-76-4

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