Welcome to LookChem.com Sign In|Join Free

CAS

  • or

95652-81-6

Post Buying Request

95652-81-6 Suppliers

Recommended suppliersmore

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

95652-81-6 Usage

Description

6-Chloro-2-methoxynicotinaldehyde is a heterocyclic derivative and a useful research chemical.

Uses

Used in Pharmaceutical Industry:
6-Chloro-2-methoxynicotinaldehyde is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to be a key component in the development of new pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 95652-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95652-81:
(7*9)+(6*5)+(5*6)+(4*5)+(3*2)+(2*8)+(1*1)=166
166 % 10 = 6
So 95652-81-6 is a valid CAS Registry Number.

95652-81-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (772747)  6-Chloro-2-methoxypyridine-3-carboxaldehyde  97%

  • 95652-81-6

  • 772747-500MG

  • 1,062.36CNY

  • Detail

95652-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-methoxypyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-CHLORO-2-METHOXY-3-PYRIDINECARBALDEHYDE

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:95652-81-6 SDS

95652-81-6Relevant articles and documents

Transformations of trichloromethyl groups during reactions of 3-trichloromethylpyridines with methoxide

Dainter, Ronald S.,Jackson, Tracey,Omar, Abdirahman H. H.,Suschitzky, Hans,Wakefield, Basil J.,Hughes, Nigel,Nelson, Anthony J.,Varvounis, George

, p. 283 - 287 (2007/10/02)

When methoxide ion attacks an unsubstituted 2- or 6-position of a 3-trichloromethylpyridine, a hydrogen shift leads to a methoxy-substituted 3-dichloromethylpyridine. Further reaction of the dichloromethyl group with methoxide gives the corresponding acetal. This type of reaction has been applied to several chlorinated 3-trichloromethylpyridines and to 3- trichloromethylpyridine itself; a convenient synthesis of the latter is 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 95652-81-6