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(E)-3-(2-fluorophenyl)but-2-enoic acid is a chemical compound with the molecular formula C10H9FO2. It is an organic molecule that belongs to the class of enoic acids, characterized by the presence of a double bond between the second and third carbon atoms in the butenoic acid backbone. The compound features a 2-fluorophenyl group attached to the third carbon, which introduces a fluorine atom into the phenyl ring. This fluorine substitution can significantly alter the chemical and physical properties of the molecule, such as its reactivity, lipophilicity, and potential biological activity. The (E) configuration indicates the geometric arrangement of the double bond, with the highest priority groups being on opposite sides of the bond. (E)-3-(2-fluorophenyl)but-2-enoic acid may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals where the introduction of fluorine can provide specific advantages.

1130-95-6

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Check Digit Verification of cas no

The CAS Registry Mumber 1130-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1130-95:
(6*1)+(5*1)+(4*3)+(3*0)+(2*9)+(1*5)=46
46 % 10 = 6
So 1130-95-6 is a valid CAS Registry Number.

1130-95-6Upstream product

1130-95-6Relevant academic research and scientific papers

Design, synthesis and SARs of novel telomerase inhibitors based on BIBR1532

Chen, Fei Hu,Liu, Chao,Liu, Xin Hua,Sheng, Xiao Bao,Zhou, Hua

, (2020)

Telomerase has become one of the new popular targets for the development of anti-tumor drugs. Based on the structural characteristics of the BIBR1532 which has entered the stage of clinical research, six series total of 64 new compounds with diverse struc

Enantioselective Hydrogenation of β,β-Disubstituted Unsaturated Carboxylic Acids under Base-Free Conditions

Yan, Qiaozhi,Kong, Duanyang,Zhao, Wei,Zi, Guofu,Hou, Guohua

, p. 2070 - 2077 (2016/03/15)

An additive-free enantioselective hydrogenation of β,β-disubstituted unsaturated carboxylic acids catalyzed by the Rh-(R,R)-f-spiroPhos complex has been developed. Under mild conditions, a wide scope of β,β-disubstituted unsaturated carboxylic acids were hydrogenated to the corresponding chiral carboxylic acids with excellent enantioselectivities (up to 99.3% ee). This methodology was also successfully applied to the synthesis of the pharmaceutical molecule indatraline.

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