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2-NITROTHIOPHENE-4-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40357-96-8

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40357-96-8 Usage

Chemical Properties

Off-white solid

Check Digit Verification of cas no

The CAS Registry Mumber 40357-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40357-96:
(7*4)+(6*0)+(5*3)+(4*5)+(3*7)+(2*9)+(1*6)=108
108 % 10 = 8
So 40357-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H3NO4S/c7-5(8)3-1-4(6(9)10)11-2-3/h1-2H,(H,7,8)/p-1

40357-96-8 Well-known Company Product Price

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

  • (A10705)  2-Nitrothiophene-4-carboxylic acid, 98%   

  • 40357-96-8

  • 250mg

  • 881.0CNY

  • Detail
  • Alfa Aesar

  • (A10705)  2-Nitrothiophene-4-carboxylic acid, 98%   

  • 40357-96-8

  • 1g

  • 3394.0CNY

  • Detail
  • Alfa Aesar

  • (A10705)  2-Nitrothiophene-4-carboxylic acid, 98%   

  • 40357-96-8

  • 5g

  • 14309.0CNY

  • Detail

40357-96-8SDS

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 5-Nitrothiophene-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Nitrothiophene-4-carboxylic 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:40357-96-8 SDS

40357-96-8Relevant academic research and scientific papers

Synthesis of highly potent and selective hetaryl ureas as integrin αVβ3-receptor antagonists

Lange, Udo E.W.,Backfisch, Gisela,Delzer, Juergen,Geneste, Herve,Graef, Claudia,Hornberger, Wilfried,Kling, Andreas,Lauterbach, Arnulf,Subkowski, Thomas,Zechel, Christian

, p. 1379 - 1382 (2007/10/03)

Solid-phase synthesis and SAR of integrin αVβ3-receptor antagonists containing a urea moiety as non-basic guanidine mimetic are described. The most potent compounds exhibited IC50 values towards αVβ3 in the nanomolar range and high selectivity versus related integrins like αIIbβ3. For selected examples efficacy in functional cellular assays is demonstrated.

Phosphorylamides, their preparation and use

-

, (2008/06/13)

A phosphorylamide derivative represented by the general formula (I): STR1 wherein R represents an amino group that may be substituted, or a salt thereof, possesses potent antibacterial activity against Helicobacter bacterium, especially Helicobacter pylori, and is useful for prevention or treatment of digestive diseases caused by Helicobacter bacterium, solely or in combination with an antacid or an acid secretion inhibitor.

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