85311-87-1 Usage
Description
(2E)-3-chloro-3-phenylprop-2-enoic acid is an unsaturated carboxylic acid with a molecular formula of C9H7ClO2. It is a colorless to pale yellow liquid and is commonly used as a building block in organic synthesis due to its molecular structure containing a double bond and a chlorine atom.
Uses
Used in Pharmaceutical Production:
(2E)-3-chloro-3-phenylprop-2-enoic acid is used as an intermediate in the production of pharmaceuticals for its potential applications in medicinal chemistry and drug discovery.
Used in Agrochemical Production:
(2E)-3-chloro-3-phenylprop-2-enoic acid is used as an intermediate in the production of agrochemicals, contributing to the development of various organic compounds.
Used in Organic Synthesis:
(2E)-3-chloro-3-phenylprop-2-enoic acid is used as a valuable intermediate in organic synthesis, enabling the synthesis of various functionalized organic compounds.
It is important to handle (2E)-3-chloro-3-phenylprop-2-enoic acid with caution due to its potential health hazards and environmental risks.
Check Digit Verification of cas no
The CAS Registry Mumber 85311-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,1 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85311-87:
(7*8)+(6*5)+(5*3)+(4*1)+(3*1)+(2*8)+(1*7)=131
131 % 10 = 1
So 85311-87-1 is a valid CAS Registry Number.
85311-87-1Relevant articles and documents
In search of the spin-delocalization effect from the correlation analysis of relative rates of the trichloromethyl-bromo-addition reactions to fourteen p-Y-substituted phenylacetylenes
Jiang, Xi-Kui,Ji, Guo-Zhen,Xie, John Rong-Yuan
, p. 3017 - 3028 (2007/10/03)
A rigorous procedure was applied to the measurement of the relative rates, i.e. k(r)(Y) = k(Y)/k(H) of trichloromethyl-bromo-addition reactions to fourteen p-Y-substituted phenylacetylenes (I-Y, with Y = F, Cl, Br, Me, t-Bu, OMe, SMe, SiMe3, CF3, CN, NO2, SOMe, COMe, and CO2Me). The reaction was run in cyclohexane under nitrogen antmosphere at 65 ± 0.5°C. All products were derived from the intermediate YC6H4C = CHCCl3 adduct radicals. Correlation analysis of these rate data seems to suggest that both a polar and a spin-delocalization effect are operating at the transition state.
