Welcome to LookChem.com Sign In|Join Free

CAS

  • or

667465-00-1

Post Buying Request

667465-00-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

667465-00-1 Usage

Uses

2-?((Cyclohexanecarbony?l)?oxy)?acetic Acid (Gabapentin EP Impurity E; Gabapentin USP Related Compound E) is a metabolite of Gabapentin (G117250), amino acid structurally related to γ-Aminobutyric Acid (GABA), designed to cross the blood brain barrier. Used as an anticonvulsant.

Check Digit Verification of cas no

The CAS Registry Mumber 667465-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,4,6 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 667465-00:
(8*6)+(7*6)+(6*7)+(5*4)+(4*6)+(3*5)+(2*0)+(1*0)=191
191 % 10 = 1
So 667465-00-1 is a valid CAS Registry Number.

667465-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohexanecarbonyloxy)acetic acid

1.2 Other means of identification

Product number -
Other names Cyclohexanecarboxylic acid,carboxymethyl ester

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:667465-00-1 SDS

667465-00-1Upstream product

667465-00-1Downstream Products

667465-00-1Relevant articles and documents

The Effect of pH Control on the Selective Ruthenium-Catalyzed Oxidation of Ethers and Alcohols with Sodium Hypochlorite

Gonsalvi, Luca,Arends, Isabel W. C. E.,Moilanen, Pasi,Sheldon, Roger A.

, p. 1321 - 1328 (2003)

Highly selective oxidations of ethers to esters or lactones and of secondary alcohols to ketones were achieved using catalytic amounts of various Ru precursors and the theoretical amount of NaOCl. Reactions were carried out in biphasic solvent mixtures at constant pH 9-9.5 via either feed-on-demand addition of HCl and NaOH or in the presence of NaHCO3/Na 2CO3 buffer. The catalyst could be easily recycled for at least 4 times with only minor loss in selectivity. Products were generally recovered by simple phase separation and evaporation of the organic solvent. The effects of catalyst precursor, additives and pH control method are also described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 667465-00-1