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3-(Carboxymethyl)-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetic acid is a complex organic compound with the chemical formula C11H10N2O4. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound with a central benzene ring fused to an imidazole ring. This specific compound features a carboxymethyl group attached to the benzimidazole core, which is further connected to an acetic acid moiety. The molecule is characterized by its 2-oxo-2,3-dihydro structure, indicating the presence of a carbonyl group and a hydrogenated ring system. 3-(CARBOXYMETHYL)-2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOL-1-YL]ACETIC ACID may have potential applications in pharmaceuticals or as a chemical intermediate due to its unique structure and functional groups.

1848-99-3

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1848-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1848-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1848-99:
(6*1)+(5*8)+(4*4)+(3*8)+(2*9)+(1*9)=113
113 % 10 = 3
So 1848-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O5/c14-9(15)5-12-7-3-1-2-4-8(7)13(11(12)18)6-10(16)17/h1-4H,5-6H2,(H,14,15)(H,16,17)/p-2

1848-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(carboxymethyl)-2-oxobenzimidazol-1-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 1.3-Bis-carboxymethyl-benzimidazolon

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:1848-99-3 SDS

1848-99-3Downstream Products

1848-99-3Relevant academic research and scientific papers

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 79, (2016/11/17)

Compounds of Formulas I-VI, including pharmaceutically acceptable salts thereof, and compositions and methods for treating human immunodeficiency virus (HIV) infection are set forth. Formula I is exemplified below: Formula (i)

SYNTHESIS OF N-CARBOXYALKYLBENZIMIDAZOLIN-2-ONES

Khalikov, S. S.,Kadyrov, Ch. Sh.,Ayupova, A. T.,Molchanov, L. V.

, p. 1251 - 1254 (2007/10/02)

The corresponding N-mono and N,N'-dicarboxyalkylbenzimidazolin-2-ones were prepared by the reaction of the sodium salts of benzimidazolin-2-one and its 1,5,6-substituted derivatives with chloroacetic acid, acrylonitrile. and γ-butyrolactone.

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