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19739-41-4

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19739-41-4 Usage

General Description

(6-Nitro-2-oxo-1,3-benzoxazol-3(2H)-yl)acetic acid is a chemical compound with a molecular formula C9H5N3O6. It is a derivative of the benzoxazolone family and contains a nitro and acetic acid group. (6-NITRO-2-OXO-1,3-BENZOXAZOL-3(2H)-YL)ACETIC ACID has the potential to be used in various chemical and pharmaceutical applications due to its unique structure and properties. It may have potential uses in various industries such as pharmaceuticals, agriculture, and materials science, but more research and testing are needed to determine its specific applications and potential benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 19739-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,3 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19739-41:
(7*1)+(6*9)+(5*7)+(4*3)+(3*9)+(2*4)+(1*1)=144
144 % 10 = 4
So 19739-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2O6/c12-8(13)4-10-6-2-1-5(11(15)16)3-7(6)17-9(10)14/h1-3H,4H2,(H,12,13)

19739-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-nitro-2-oxo-1,3-benzoxazol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names 2-(6-nitro-2-oxo-benzooxazol-3-yl)acetate

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:19739-41-4 SDS

19739-41-4Downstream Products

19739-41-4Relevant articles and documents

Development of benzo[d]oxazol-2(3H)-ones derivatives as novel inhibitors of Mycobacterium tuberculosis InhA

Pedgaonkar, Ganesh S.,Sridevi, Jonnalagadda Padma,Jeankumar, Variam Ullas,Saxena, Shalini,Devi, Parthiban Brindha,Renuka, Janupally,Yogeeswari, Perumal,Sriram, Dharmarajan

, p. 6134 - 6145 (2015/02/19)

A series of twenty seven substituted 2-(2-oxobenzo[d]oxazol-3(2H)-yl)acetamide derivatives were designed based on our earlier reported Mycobacterium tuberculosis (MTB) enoyl-acyl carrier protein reductase (InhA) lead. Compounds were evaluated for MTB InhA inhibition study, in vitro activity against drug-sensitive and -resistant MTB strains, and cytotoxicity against RAW 264.7 cell line. Among the compounds tested, 2-(6-nitro-2-oxobenzo[d]oxazol-3(2H)-yl)-N-(5-nitrothiazol-2-yl)acetamide (30) was found to be the most promising compound with IC50 of 5.12 ± 0.44 μM against MTB InhA, inhibited drug sensitive MTB with MIC 17.11 μM and was non-cytotoxic at 100 μM. The interaction with protein and enhancement of protein stability in complex with compound 30 was further confirmed biophysically by differential scanning fluorimetry.

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