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3-(4-bromophenyl)-3-phenyl-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80272-20-4

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80272-20-4 Usage

Derivative of

propionic acid

Structure

consists of a phenyl group and a bromophenyl group attached to the third carbon of the propionic acid backbone

Main uses

organic synthesis, pharmaceutical research

Potential uses

development of new drugs, study of structure-activity relationships

Additional uses

reference standard in analytical chemistry, quality control processes.

Check Digit Verification of cas no

The CAS Registry Mumber 80272-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,7 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80272-20:
(7*8)+(6*0)+(5*2)+(4*7)+(3*2)+(2*2)+(1*0)=104
104 % 10 = 4
So 80272-20-4 is a valid CAS Registry Number.

80272-20-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenyl)-3-phenyl-propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-bromophenyl)-3-phenyl-propionic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80272-20-4 SDS

80272-20-4Relevant academic research and scientific papers

NEW DIFLUOROKETAMIDE DERIVATIVES

-

Page/Page column 38-39; 40, (2016/12/01)

The invention provides novel compounds having the general formula (I) wherein R1, R2, R3, R4, R5, R6, R7, R8 and R9 are as described herein, compositions including the compounds and methods of using the compounds.

Development of modifiable bidentate amino oxazoline directing group for Pd-catalyzed arylation of secondary C-H bonds

Chen, Kang,Li, Zhao-Wei,Shen, Peng-Xiang,Zhao, Hong-Wei,Shi, Zhang-Jie

supporting information, p. 7389 - 7393 (2015/05/13)

Abstract A novel bidentate α-amino oxazolinyl directing group has been developed. Different from previous directing groups, this newly designed directing group was easily prepared from amino acids and modified in structure. This auxiliary preferentially effects functionalization at secondary C(sp3)-H bonds, rather than at aryl C(sp2)-H bonds. The diastereoselectivity of direct arylation between geminal secondary C(sp3)-H bonds in linear molecules has also been realized for the first time with a chiral directing group by remote chirality relay. Two diastereoisomers are produced with the same chiral source by changing the substituents of substrates and aryl halides. A new direction: A multifunctional amino oxazoline directing group that is readily available from amino acids, has been developed, which can induce chemo-, regio- and diastereoselectivity in secondary C(sp3)-H arylation reactions. Furthermore, this directing group is removable and modifiable. Steric control and counterions play important roles in the relayed chirality transfer.

Ring-substituted histaprodifen analogues as partial agonists for histamine H1 receptors: Synthesis and structure-activity relationships

Elz, Sigurd,Kramer, Kai,Leschke, Christian,Schunack, Walter

, p. 41 - 52 (2007/10/03)

Thirteen racemic benzene ring-substituted analogues of histaprodifen (8a; 2-[2-(3,3-diphenylpropyl)-1H-imidazol-4-yl]ethanamine), a novel lead for potent and selective histamine H1-receptor agonists, have been prepared from substituted 4,4-diphenylbutyronitriles 5 via cyclization of the corresponding methyl butyrimidates 6 with 2-oxo-4-phthalimido-1-butyl acetate in liquid ammonia, followed by deprotection. Nitriles 5 were accessible by alkylation of either substituted diphenylmethanes with 3-bromopropionitrile or diethyl malonate with substituted 1-chloro-diphenylmethanes and subsequent standard reactions. The title compounds 8 displayed partial agonism on conctractile H1 receptors of the guinea-pig ileum (E(max) = 2-98% relative to histamine) and, compared with the endogenous agonist, were endowed with agonist potencies of 4-92%. The meta fluorinated (8c) and meta chlorinated (8f) analogues showed the highest relative potency in this series (95% confidence limits 85-99% and 78-102%), but did not exceed the value of the lead 8a (99- 124%). Compound 8c (2-[2-[3-(3-fluorophenyl)-3-phenylpropyl]-1H-imidazol-4- yl]ethanamine) was a partial agonist at contractile H1 receptors of the guinea-pig aorta (relative potency 154% vs. 100% for histamine) and at relaxation-mediating endothelial H1 receptors of the rat aorta (relative potency 556% vs. 100% for histamine) and matched with the functional behaviour of 8a. Agonism observed for each compound was sensitive to blockade by the selective H1-receptor antagonist mepyramine (pA2 ? 9 (guinea-pig) and pA2 ? 8 (rat aorta)). All histaprodifen analogues 8 stimulated neither histaminergic H2/H3 nor cholinergic M3 receptors. They displayed only low to moderate affinity for these sites (H2: pD'2 3/M3: pA2 1-receptor agonist, viz. 2- phenylhistamine. (C) 2000 Editions scientifiques et medicales Elsevier SAS.

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