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10351-75-4

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10351-75-4 Usage

Uses

Benzimidazole-5,6-dicarboxylic acid is a important organic intermediate. It is used in agrochemical, pharmaceutical and dyestuff field.

Check Digit Verification of cas no

The CAS Registry Mumber 10351-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10351-75:
(7*1)+(6*0)+(5*3)+(4*5)+(3*1)+(2*7)+(1*5)=64
64 % 10 = 4
So 10351-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2O4/c12-8(13)4-1-6-7(11-3-10-6)2-5(4)9(14)15/h1-3H,(H,10,11)(H,12,13)(H,14,15)

10351-75-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L14754)  Benzimidazole-5,6-dicarboxylic acid, 97%   

  • 10351-75-4

  • 1g

  • 521.0CNY

  • Detail
  • Alfa Aesar

  • (L14754)  Benzimidazole-5,6-dicarboxylic acid, 97%   

  • 10351-75-4

  • 5g

  • 1854.0CNY

  • Detail

10351-75-4SDS

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 1H-Benzo[d]imidazole-5,6-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names Benzimidazole-5,6-dicarboxylic 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:10351-75-4 SDS

10351-75-4Relevant articles and documents

Symmetrical non-chelating poly-N-heterocyclic carbenes

Chen, Ying-Hsuan,Peng, Kai-En,Lee, Gene-Hsiang,Peng, Shie-Ming,Chiu, Ching-Wen

, p. 62789 - 62792 (2014)

A facile synthetic protocol, which utilized dehydrative condensation of phthalic anhydride and primary amines, for symmetrical non-chelating poly-N-heterocyclic carbene ligands was established. With the designed bi-functional building block, poly-NHC ligands having various denticities and geometries could be readily achieved by varying the structure of poly-amino compounds. Examination of catalytic activity of a series of poly-NHC-Ni complexes revealed the lack of electronic interference among NHC-metal units. This journal is

Size-expanded analogues of dG and dC: Synthesis and pairing properties in DNA

Liu, Haibo,Gao, Jianmin,Kool, Eric T.

, p. 639 - 647 (2007/10/03)

(Chemical Equation Presented) We describe the completion of the set of four benzo-fused expanded DNA (xDNA) nucleoside analogues. We previously reported the development of benzo-fused analogues of dA and dT and their inclusion in an exceptionally stable n

GASTIN AND CCK RECEPTOR LIGANDS

-

, (2008/06/13)

Compounds of formula (Ia), (Ib), or (Ic), wherein A represents a group having two fused rings, or a group of formula (Id), R 1 (m) represents up to 6 substituents, K represents--O--,--S--,--CH 2--,--N(R 2)--or--N(COR 2)--, in which R 2 is H or C 1 to C 3 alkyl, W is a carbonyl, sulfonyl or sulfinyl group, provided that at least one of W and X contains carbonyl, Y and Z are as given in the description, and their pharmaceutically acceptable salts are ligands at CCK and/or gastrin receptors. STR1

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