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(Z)-Methyl 3-((2'-(N'-hydroxycarbaMiMidoyl)biphenyl-4-yl)Methyl)-2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-4-carboxylate is a complex chemical compound characterized by a benzimidazole ring system, a carboxylate group, and a biphenyl moiety. (Z)-Methyl 3-((2'-(N'-hydroxycarbaMiMidoyl)biphenyl-4-yl)Methyl)-2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-4-carboxylate may hold potential pharmaceutical applications due to the known biological activities of benzimidazole derivatives, which include anti-inflammatory, anti-cancer, and anti-microbial properties. The carboxylate group present in its structure suggests possible drug-like characteristics, enabling it to engage in various chemical reactions and interactions within biological systems. As such, (Z)-Methyl 3-((2'-(N'-hydroxycarbaMiMidoyl)biphenyl-4-yl)Methyl)-2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-4-carboxylate warrants further investigation and development in medicinal chemistry.

1499167-72-4

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1499167-72-4 Usage

Uses

Used in Pharmaceutical Industry:
(Z)-Methyl 3-((2'-(N'-hydroxycarbaMiMidoyl)biphenyl-4-yl)Methyl)-2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-4-carboxylate is used as a potential pharmaceutical agent for its possible anti-inflammatory, anti-cancer, and anti-microbial properties. The presence of the carboxylate group may facilitate its interaction with biological targets, enhancing its therapeutic potential.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (Z)-Methyl 3-((2'-(N'-hydroxycarbaMiMidoyl)biphenyl-4-yl)Methyl)-2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-4-carboxylate serves as a subject for further study and development. Its complex molecular structure and the presence of functional groups make it a promising candidate for the design and synthesis of new drugs with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1499167-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,9,1,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1499167-72:
(9*1)+(8*4)+(7*9)+(6*9)+(5*1)+(4*6)+(3*7)+(2*7)+(1*2)=224
224 % 10 = 4
So 1499167-72-4 is a valid CAS Registry Number.

1499167-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-((2'-(N'-hydroxycarbamimidoyl)biphenyl-4-yl)methyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names (Z)-methyl 3-((2'-(N'-hydroxycarbamimidoyl)biphenyl-4-yl)methyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carboxylate

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:1499167-72-4 SDS

1499167-72-4Downstream Products

1499167-72-4Relevant academic research and scientific papers

Synthesis of azilsartan and its selected potential impurities

Radl, Stanislav,Cerny, Josef,Stach, Jan,Holec, Jan,Pisa, Ondrej,Gablikova, Zuzana

, p. 929 - 936 (2013/08/23)

Synthesis of angiotensin II AT1 receptor antagonist azilsartan is described. The results include reinvestigation of the described process as well as its novel modification. This new process includes transformation of the CN group into amidoxime moiety by aqueous hydroxylamine, its treatment with alkyl chloroformates and a base-initiated cyclization of the formed (alkoxycarbonyl-oxy)carbamimidoyl intermediates. Several so far undescribed side-products were identified and some of them were synthesized and duly characterized as potential impurities.

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