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99277-71-1

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99277-71-1 Usage

Chemical Properties

Solid

Uses

Different sources of media describe the Uses of 99277-71-1 differently. You can refer to the following data:
1. 4-Bromo-2-nitrobenzoic acid is an intermediate in the synthesis of Lonafarnib (L469445), a potential anticancer agent.
2. Undergoes Negishi-type coupling with dimethylzinc in the presence of palladium-phosphine catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 99277-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,7 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99277-71:
(7*9)+(6*9)+(5*2)+(4*7)+(3*7)+(2*7)+(1*1)=191
191 % 10 = 1
So 99277-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrNO4/c8-4-1-2-5(7(10)11)6(3-4)9(12)13/h1-3H,(H,10,11)/p-1

99277-71-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (H27541)  4-Bromo-2-nitrobenzoic acid, 97%   

  • 99277-71-1

  • 1g

  • 425.0CNY

  • Detail
  • Alfa Aesar

  • (H27541)  4-Bromo-2-nitrobenzoic acid, 97%   

  • 99277-71-1

  • 5g

  • 1366.0CNY

  • Detail

99277-71-1SDS

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 4-Bromo-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-nitro-4-bromobenzoic 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:99277-71-1 SDS

99277-71-1Relevant articles and documents

Synthesis and solid-phase purification of anthranilic sulfonamides as CCK-2 ligands

Woods, Craig R.,Hack, Michael D.,Allison, Brett D.,Phuong, Victor K.,Rosen, Mark D.,Morton, Magda F.,Prendergast, Clodagh E.,Barrett, Terrance D.,Shankley, Nigel P.,Rabinowitz, Michael H.

, p. 6905 - 6909 (2008/04/07)

A novel strategy for the synthesis of cholecystokinin-2 receptor ligands was developed. The route employs a solution-phase synthesis of a series of anthranilic sulfonamides followed by a resin capture purification strategy to produce multi-milligram quant

GLYCOGEN PHOSPHORYLASE INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF

-

Page/Page column 87-88, (2010/11/30)

The invention relates to glycogen phosphorylase inhibitor compounds, pharmaceutical compositions of these compounds, methods of treatment using the pharmaceutical compositions to treat diabetes, conditions associated with diabetes, and/or tissue ischemia,

Oxidation of 4-halo-2-nitrotoluene with tetrabutylammonium permanganate in pyridine: Development and safety evaluation

Deng, Xiaohu,Stefanick, Stephen,Pippel, Marna C. W.,Mani, Neelakandha S.

, p. 1287 - 1291 (2012/12/23)

4-Halo-2-nitrobenzoic acids are synthesized by oxidation of 4-halo-2-nitrotoluene with tetrabutylammonium permanganate (TBAP) in pyridine in multigram quantities. A significant induction period is observed at room temperature, and the vigorous exothermic

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