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3894-09-5

3894-09-5

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3894-09-5 Usage

Chemical Properties

GREY CRYSTALLINE POWDER

Uses

α-Cyclohexyl-benzeneacetic Acid is a useful synthetic intermediate. It was used as one of the reactants to prepare phenylureidobenzazepinones as cholecystokinin-B receptor antagonists. It can also be used to synthesize benzimidazole derivatives as potent AMP-activated protein kinase activators.

Check Digit Verification of cas no

The CAS Registry Mumber 3894-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3894-09:
(6*3)+(5*8)+(4*9)+(3*4)+(2*0)+(1*9)=115
115 % 10 = 5
So 3894-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O2/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2,(H,15,16)/p-1/t13-/m1/s1

3894-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexyl-2-phenylacetic acid

1.2 Other means of identification

Product number -
Other names Cyclohexylphenylacetic 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:3894-09-5 SDS

3894-09-5Relevant articles and documents

Oxidative cleavage of α-aryl aldehydes using iodosylbenzene

Havare, Nizam,Plattner, Dietmar A.

, p. 5078 - 5081,4 (2020/09/15)

We found that α-aryl aldehydes can be cleaved to chain-shortened carbonyl compounds and formaldehyde by various iodosylbenzene complexes. A mechanistic scheme is presented that accounts for the loss of one carbon atom. Formaldehyde is further oxidized to CO and CO2 under the reaction conditions.

Discovery of new C3aR ligands. Part 2: Amino-piperidine derivatives

Denonne, Frederic,Binet, Sophie,Burton, Maggi,Collart, Philippe,Defays, Sabine,Dipesa, Alan,Eckert, Maria,Giannaras, Alexander,Kumar, Seema,Levine, Beth,Nicolas, Jean-Marie,Pasau, Patrick,Pegurier, Cecile,Preda, Dorin,Van houtvin, Nathalie,Volosov, Andrew,Zou, Dong

, p. 3262 - 3265 (2008/02/08)

The synthesis and structure-activity relationships against the C3a receptor of a series of substituted aminopiperidine derivatives are reported. DMPK properties and functional activities of selected compounds are described. The compounds obtained are the first non-arginine ligands of C3aR.

Oxidative decarboxylation of arylacetic acids mediated by peroxysulfur intermediate generated from 2-nitrobenzenesulfonyl chloride and superoxide

Kim II, Yong,Kim, Yong Hae

, p. 639 - 642 (2007/10/03)

The oxidative decarboxylation of aryl, α, α-diaryl, or arylalkylacetic acids has been achieved by a 2-nitrobenzenesulfonyl peroxy radical intermediate (I) generated by the reaction of 2-nitrobenzenesulfonyl chloride with potassium superoxide at -20°C in dry acetonitrile.

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