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22282-96-8

22282-96-8

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22282-96-8 Usage

Chemical Properties

Yellow Solid

Check Digit Verification of cas no

The CAS Registry Mumber 22282-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,8 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22282-96:
(7*2)+(6*2)+(5*2)+(4*8)+(3*2)+(2*9)+(1*6)=98
98 % 10 = 8
So 22282-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrN2O2/c1-4-5(9(10)11)2-3-6(7)8-4/h2-3H,1H3

22282-96-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H64299)  6-Bromo-2-methyl-3-nitropyridine, 97%   

  • 22282-96-8

  • 5g

  • 304.0CNY

  • Detail

  • Alfa Aesar

  • (H64299)  6-Bromo-2-methyl-3-nitropyridine, 97%   

  • 22282-96-8

  • 25g

  • 1245.0CNY

  • Detail

  • Aldrich

  • (758175)  6-Bromo-2-methyl-3-nitropyridine  97%

  • 22282-96-8

  • 758175-5G

  • 768.69CNY

  • Detail

22282-96-8SDS

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 2-Bromo-6-methyl-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 6-Bromo-2-methyl-3-nitropyridine

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:22282-96-8 SDS

22282-96-8Relevant articles and documents

Azaindoles: Moderately basic P1 groups for enhancing the selectivity of thrombin inhibitors

Sanderson, Philip E. J.,Stanton, Matthew G.,Dorsey, Bruce D.,Lyle, Terry A.,McDonough, Colleen,Sanders, William M.,Savage, Kelly L.,Naylor-Olsen, Adel M.,Krueger, Julie A.,Lewis, S. Dale,Lucas, Bobby J.,Lynch, Joseph J.,Yan, Youwei

, p. 795 - 798 (2007/10/03)

Starting from a 2-amino-6-methylpyridine P1 group and following a strategy of enlarging it whilst reducing its polarity, we have developed a series of potent, moderately basic azaindoles which are intrinsically much more selective for thrombin versus tryp

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