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54231-35-5

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54231-35-5 Usage

Chemical Properties

light brown crystal powder or liquid

Uses

A specialty product for proteomics research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 54231-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,3 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54231-35:
(7*5)+(6*4)+(5*2)+(4*3)+(3*1)+(2*3)+(1*5)=95
95 % 10 = 5
So 54231-35-5 is a valid CAS Registry Number.

54231-35-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • TCI America

  • (F0981)  3-Fluoro-2-nitropyridine  >98.0%(GC)

  • 54231-35-5

  • 1g

  • 990.00CNY

  • Detail
  • Alfa Aesar

  • (H33813)  3-Fluoro-2-nitropyridine, 96%   

  • 54231-35-5

  • 250mg

  • 459.0CNY

  • Detail
  • Alfa Aesar

  • (H33813)  3-Fluoro-2-nitropyridine, 96%   

  • 54231-35-5

  • 1g

  • 1170.0CNY

  • Detail
  • Alfa Aesar

  • (H33813)  3-Fluoro-2-nitropyridine, 96%   

  • 54231-35-5

  • 5g

  • 3549.0CNY

  • Detail

54231-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Fluoro-2-Nitropyridine

1.2 Other means of identification

Product number -
Other names 3-Fluoro-2-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:54231-35-5 SDS

54231-35-5Upstream product

54231-35-5Relevant articles and documents

Cross-coupling reaction of 2-halo1-methyl-1H-imidazo[4,5-b]pyridine offers a new synthetic route to mutagenic heterocyclic amine-PHIP and DMIP

Sajith, Ayyiliath M.,Muralidharan, Arayambath,Karuvalam, Ranjith P.,Haridas, Karickal R.

, p. 361 - 364 (2013/07/26)

A modified synthetic approach to the synthesis of heterocyclic food mutagens, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PHIP) and 2-amino-1,6-dimethylimidazo[4,5-b]pyridine (DMIP) is reported. This route highlights an optimized palladium catalysed Buchwald cross-coupling of 2-halo-1-methyl-imidazo[4,5-b]pyridine with benzophenoneimine followed by acidic hydrolysis to yield compound 7. Using finely tailored conditions, Suzuki cross-coupling reactions with highly efficient catalytic systems were performed as the final step on 8 to introduce the aryl group and methyl group on the heterocyclic core.

Synthesis and Spectral Data of Pyrido-as-triazines

Ple, N.,Queguiner, G.

, p. 475 - 476 (2007/10/02)

The pyrido-as-triazine and its 3-phenyl derivatives were prepared via cyclisation with polyphosphoric acid of suitable 3-substituted 2-aminopyridines obtained by reduction of the corresponding 2-nitropyridines.The 3-substituted 2-nitropyridines wer

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