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Propanoic acid, 3-oxo-3-(phenylamino)-, hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15601-64-6

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15601-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15601-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,0 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15601-64:
(7*1)+(6*5)+(5*6)+(4*0)+(3*1)+(2*6)+(1*4)=86
86 % 10 = 6
So 15601-64-6 is a valid CAS Registry Number.

15601-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl malonamic acid hydrazide

1.2 Other means of identification

Product number -
Other names malonanilic acid hydrazide

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:15601-64-6 SDS

15601-64-6Relevant academic research and scientific papers

Design and synthesis of bis-amide and hydrazide-containing derivatives of malonic acid as potential HIV-1 integrase inhibitors

Sechi, Mario,Azzena, Ugo,Delussu, Maria Paola,Dallocchio, Roberto,Dessi, Alessandro,Cosseddu, Alessia,Pala, Nicolino,Neamati, Nouri

experimental part, p. 2442 - 2461 (2009/04/05)

HIV-1 integrase (IN) is an attractive and validated target for the development of novel therapeutics against AIDS. In the search for new IN inhibitors, we designed and synthesized three series of bis-amide and hydrazide-containing derivatives of malonic acid. We performed a docking study to investigate the potential interactions of the title compounds with essential amino acids on the IN active site.

Efficient synthesis of 4-ethoxycarbonyl pyrazolin-5-one derivatives

Jung, Jae C.,Watkins, E Blake,Avery, Mitchell A.

, p. 3767 - 3777 (2007/10/03)

Concise and efficient methods for the preparation of 3-substituted 4-ethoxycarbonylpyrazolin-5-ones are described. The synthetic strategies involve carbon-acylation in the presence of base, followed by ring cyclization with hydrazine or hydrazine monohydrochloride.

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