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Glycine, N-(4-nitrobenzoyl)-, hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139645-87-7

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139645-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139645-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,4 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 139645-87:
(8*1)+(7*3)+(6*9)+(5*6)+(4*4)+(3*5)+(2*8)+(1*7)=167
167 % 10 = 7
So 139645-87-7 is a valid CAS Registry Number.

139645-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitro-benzoyl)-glycine hydrazide

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzaminoessigsaeurehydrazid

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:139645-87-7 SDS

139645-87-7Relevant academic research and scientific papers

Synthesis and antiviral activities of novel acylhydrazone derivatives targeting HIV-1 capsid protein

Tian, Baohe,He, Meizi,Tang, Shixing,Hewlett, Indira,Tan, Zhiwu,Li, Jiebo,Jin, Yinxue,Yang, Ming

experimental part, p. 2162 - 2167 (2009/12/25)

HIV-1 capsid protein (CA) plays important roles in the viral replication cycle. A number of acylhydrazone derivatives that act as inhibitors of HIV-1 CA assembly, were designed and synthesized. The synthesized compounds were tested for their antiviral activities and cytotoxicities using CEM cells. Some derivatives also were assayed for their ability to inhibit HIV-1 CA assembly in vitro. Among them, compounds 14f and 14i display the most promising potency with EC50 values of 0.21 and 0.17 μΜ, respectively.

Inhibitors of bacterial cystathionine β-lyase: Leads for new antimicrobial agents and probes of enzyme structure and function

Ejim, Linda J.,Blanchard, Jan E.,Koteva, Kalinka P.,Sumerfield, Rachael,Elowe, Nadine H.,Chechetto, Jonathan D.,Brown, Eric D.,Junop, Murray S.,Wright, Gerard D.

, p. 755 - 764 (2007/10/03)

The biosynthesis of methionine is an attractive antibiotic target given its importance in protein and DNA metabolism and its absence in mammals. We have performed a high-throughput screen of the methionine biosynthesis enzyme cystathionine β-lyase (CBL) a

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