Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6627-68-5

Post Buying Request

6627-68-5 Suppliers

Recommended suppliersmore

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

6627-68-5 Usage

General Description

2-(1-Cyclohexenyl)-butyric acid, also known as 2-Cyclohexenylbutanoic acid, is a chemical compound with a molecular formula C10H16O2. It is a carboxylic acid with a cyclohexene ring and a butyric acid side chain. 2-(1-CYCLOHEXENYL)-BUTYRIC ACID is used in the synthesis of pharmaceuticals and agricultural chemicals, and it has potential applications in the fragrance and flavor industry. It is also being studied for its potential anti-inflammatory and anti-cancer properties. 2-(1-Cyclohexenyl)-butyric acid is a colorless to pale yellow liquid at room temperature and is typically stored and handled in a cool, dry environment.

Check Digit Verification of cas no

The CAS Registry Mumber 6627-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6627-68:
(6*6)+(5*6)+(4*2)+(3*7)+(2*6)+(1*8)=115
115 % 10 = 5
So 6627-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H10ClN3OS/c18-13-8-6-11(7-9-13)10-14-16(22)21-15(19-20-17(21)23-14)12-4-2-1-3-5-12/h1-10H/b14-10-

6627-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohexen-1-yl)butanoic acid

1.2 Other means of identification

Product number -
Other names 2-cyclohex-1-enyl-butyric 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:6627-68-5 SDS

6627-68-5Relevant articles and documents

SYNTHETIS OF CYCLIC AND ACYCLIC β,γ-UNSATURATED CARBOXYLIC ACIDS VIA AN E1-TYPE IONIZATION/ELIMINATION OF β-LACTONES

Black, T. Howard,Eisenbeis, Shane A.,McDermott, Todd S.,Maluleka, Stephen L.

, p. 2307 - 2316 (2007/10/02)

Cyclic and acyclic ketones were converted in three steps into 3-alkenoic acids, bearing a variety of substituents in the α-position.The sequence, involving ionization/elimination of a β-lactone, affords high yields of pure products uncontaminated with conjugated isomers.Support for an E1-type mechanism is also provided.

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 6627-68-5