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49773-26-4

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49773-26-4 Usage

General Description

4-ETHOXY-N-HYDROXY-BENZAMIDINE is a chemical compound with the molecular formula C9H11N2O2. It is an organic amide derivative with a benzene ring and a hydroxy group attached to the nitrogen atom. 4-ETHOXY-N-HYDROXY-BENZAMIDINE is used in pharmaceutical research and development as a potential drug candidate for various therapeutic applications. It may have anticoagulant, antithrombotic, or anti-inflammatory properties due to its ability to inhibit specific enzymes or proteins in the body. The ethoxy group in the molecule also contributes to its pharmacological activity and can influence its bioavailability and metabolism within the body. Further research is needed to fully understand the pharmacological and therapeutic potential of 4-ETHOXY-N-HYDROXY-BENZAMIDINE.

Check Digit Verification of cas no

The CAS Registry Mumber 49773-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,7 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49773-26:
(7*4)+(6*9)+(5*7)+(4*7)+(3*3)+(2*2)+(1*6)=164
164 % 10 = 4
So 49773-26-4 is a valid CAS Registry Number.

49773-26-4SDS

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 4-Ethoxy-N'-hydroxybenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names 4-ETHOXY-N-HYDROXY-BENZAMIDINE

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:49773-26-4 SDS

49773-26-4Upstream product

49773-26-4Relevant articles and documents

In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis

Deb, Pran Kishore,Al-Shar’i, Nizar A.,Venugopala, Katharigatta N.,Pillay, Melendhran,Borah, Pobitra

, p. 869 - 884 (2021/06/11)

The alarming increase in multi- and extensively drug-resistant (MDR and XDR) strains of Mycobacterium tuberculosis (MTB) has triggered the scientific community to search for novel, effective, and safer therapeutics. To this end, a series of 3,5-disubstitu

Design, microwave assisted synthesis and characterization of substituted 1,2,4-oxadiazole analogues as promising pharmacological agents

Venugopala, Katharigatta N.

, p. 1767 - 1770 (2017/06/27)

Microwave assisted synthesis of a series of 3,5-disubstituted-1,2,4-oxadiazole analogues (3a-j) has been achieved between 5-(chloromethyl)-3-substituted phenyl-1,2,4-oxadiazoles (2a-j) and substituted benzophenone in presence of potassium carbonate in ace

1,2,4-Oxadiazoles. IV. Synthesis and pharmacological properties of a series of substituted aminoalkyl-1,2,4-oxadiazoles.

PALAZZO,TAVELLA,STRANI,SILVESTRINI

, p. 351 - 367 (2007/10/05)

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