Welcome to LookChem.com Sign In|Join Free
  • or
2-Bromoadipic acid is an organic compound with the chemical formula C6H9BrO4. It is a white crystalline solid that is soluble in water and various organic solvents. 2-Bromoadipic acid is a derivative of adipic acid, where one of the hydrogen atoms on the second carbon has been replaced by a bromine atom. 2-Bromoadipic acid is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and specialty polymers. It is also employed in the production of certain dyes and pigments. Due to its reactivity, it is important to handle 2-bromoadipic acid with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

3269-62-3

Post Buying Request

3269-62-3 Suppliers

Recommended suppliers

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

3269-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3269-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3269-62:
(6*3)+(5*2)+(4*6)+(3*9)+(2*6)+(1*2)=93
93 % 10 = 3
So 3269-62-3 is a valid CAS Registry Number.

3269-62-3SDS

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-bromohexanedioic acid,6-ethyl ester

1.2 Other means of identification

Product number -
Other names 2-bromo-adipic 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:3269-62-3 SDS

3269-62-3Relevant academic research and scientific papers

Mercaptoacyl matrix metalloproteinase inhibitors: The effect of substitution at the mercaptoacyl moiety

Baxter, Andrew D.,Bhogal, Ranjev,Bird, John B.,Buckley, George M.,Gregory, David S.,Hedger, Paul C.,Manallack, David T.,Massil, Tracy,Minton, Kevin J.,Montana, John G.,Neidle, Stephen,Owen, David A.,Watson, Robert J.

, p. 2765 - 2770 (2007/10/03)

The in vitro potency of orally-active mercaptoacyl matrix metalloproteinase inhibitors is increased by the introduction of appropriate substitutents on the mercaptoacyl moiety.

Synthesis of α-haloadipic acids from 1,2-cyclohexanedione

Starostin,Mazurchik,Ignatenko,Nikishin

, p. 917 - 918 (2007/10/02)

A preparative method for the synthesis of α-haloadipic acids 4a-c by oxidative cleavage of 1,2-cyclohexanedione (1) in copper(II) halide/hydrogen peroxide or copper(II) halide (catalyst)/alkali metal halide/hydrogen peroxide system is reported.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3269-62-3