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7169-97-3

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7169-97-3 Usage

Chemical Properties

White powder

Uses

2-Acetamido-5-bromopyridine is a chemical reagent used in the synthesis of novel Bcr-Abl inhibitors with diacylated piperazine felxible linkers. Also used to produce hetero-monocyclic derivatives as even more potent inhibitors of BCR-ABL.

Check Digit Verification of cas no

The CAS Registry Mumber 7169-97-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7169-97:
(6*7)+(5*1)+(4*6)+(3*9)+(2*9)+(1*7)=123
123 % 10 = 3
So 7169-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrN2O/c1-5(11)10-7-3-2-6(8)4-9-7/h2-4H,1H3,(H,9,10,11)

7169-97-3 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (H27456)  2-Acetamido-5-bromopyridine, 98%   

  • 7169-97-3

  • 1g

  • 214.0CNY

  • Detail
  • Alfa Aesar

  • (H27456)  2-Acetamido-5-bromopyridine, 98%   

  • 7169-97-3

  • 10g

  • 1018.0CNY

  • Detail
  • Aldrich

  • (646407)  2-Acetylamino-5-bromopyridine  98%

  • 7169-97-3

  • 646407-1G

  • 253.89CNY

  • Detail
  • Aldrich

  • (646407)  2-Acetylamino-5-bromopyridine  98%

  • 7169-97-3

  • 646407-10G

  • 1,102.14CNY

  • Detail

7169-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Acetamido-5-bromopyridine

1.2 Other means of identification

Product number -
Other names N-(5-bromopyridin-2-yl)acetamide

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:7169-97-3 SDS

7169-97-3Relevant articles and documents

A new, one-step, effective protocol for the iodination of aromatic and heterocyclic compounds via aprotic diazotization of amines

Krasnokutskaya, Elena A.,Semenischeva, Nadya I.,Filimonov, Victor D.,Knochel, Paul

, p. 81 - 84 (2008/01/03)

We have developed a convenient one-step preparation of aromatic and some heterocyclic iodides by the sequential diazotization-iodination of the aromatic amines with a KI/NaNO2/p-TsOH system in acetonitrile at room temperature. This method has general character and allows aryl iodides with either donor or acceptor substituents in various positions to be obtained from the corresponding amines in 50-90% yield. Georg Thieme Verlag Stuttgart.

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