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1438-96-6

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1438-96-6 Usage

Uses

2-(2-Oxocyclohexyl)acetic acid is used as a reactant in the preparation of β-carbolines via diastereo- and enantioselective Bronsted acid catalyzed N-acyliminium cyclization cascades of tryptamines and keto acids/esters.

Check Digit Verification of cas no

The CAS Registry Mumber 1438-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1438-96:
(6*1)+(5*4)+(4*3)+(3*8)+(2*9)+(1*6)=86
86 % 10 = 6
So 1438-96-6 is a valid CAS Registry Number.

1438-96-6SDS

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 2-(2-oxocyclohexyl)acetic acid

1.2 Other means of identification

Product number -
Other names Cyclohexaneacetic acid,2-oxo

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:1438-96-6 SDS

1438-96-6Relevant articles and documents

Bicyclic brominated furanones: A new class of quorum sensing modulators that inhibit bacterial biofilm formation

Yang, Sijie,Abdel-Razek, Osama A.,Cheng, Fei,Bandyopadhyay, Debjyoti,Shetye, Gauri S.,Wang, Guirong,Luk, Yan-Yeung

, p. 1313 - 1317 (2014)

Both natural and synthetic brominated furanones are known to inhibit biofilm formation by bacteria, but their toxicity to mammalian cells is often not reported. Here, we designed and synthesized a new class of brominated furanones (BBFs) that contained a

First and Highly Stereoselective Synthesis of Both Enantiomers of Octahydroindole-2-phosphonic Acid (OicP)

Viveros-Ceballos, José Luis,Martínez-Toto, Erick Iván,Eustaquio-Armenta, César,Cativiela, Carlos,Ordó?ez, Mario

, p. 6781 - 6787 (2017/12/07)

We report the first stereoselective synthesis of (2R,3aR,7aR)- and (2S,3aS,7aS)-octahydroindole-2-phosphonic acid 2 (OicP derivatives). The key points are the highly diastereoselective synthesis of cis-fused bicyclic (3aR,7aR)- and (3aS,7aS)-pyrrolidin-2-ones 4 through a dynamic kinetic resolution of racemic γ-keto acid (±)-5 with (R)- and (S)-phenylglycinol via Meyers' bicyclic lactams, and the highly diastereoselective addition of trimethyl phosphite to the N-acyliminium ions 3 obtained from 4.

NOVEL COMPOUNDS

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Page/Page column 52; 53, (2015/12/17)

Disclosed are novel retinoid-related orphan receptor gamma (RORγ) modulators and their use in the treatment of diseases mediated by RORγ.

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