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Hydrazinecarboxamide, N-2-pyridinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64341-20-4

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64341-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64341-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64341-20:
(7*6)+(6*4)+(5*3)+(4*4)+(3*1)+(2*2)+(1*0)=104
104 % 10 = 4
So 64341-20-4 is a valid CAS Registry Number.

64341-20-4SDS

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 4-pyridin-2-ylsemicarbazide

1.2 Other means of identification

Product number -
Other names 4-[2]pyridyl semicarbazide

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:64341-20-4 SDS

64341-20-4Downstream Products

64341-20-4Relevant academic research and scientific papers

Synthesis, cytotoxicity, and in vivo antitumor activity study of parthenolide semicarbazones and thiosemicarbazones

Du, Guohua,Jia, Xinxin,Li, Yan,Liu, Qi,Wang, Shiyi,Zeng, Binglin,Zhang, Chen

, (2020/05/29)

Parthenolide is an important sesquiterpene lactone with potent anticancer activities. In order to further improve its biological activity, a series of parthenolide semicarbazone or thiosemicarbazone derivatives was synthesized and evaluated for their anti

Preparation of substituted semicarbazides from corresponding amines and hydrazines via phenyl carbamates

Hron, Rebecca,Jursic, Branko S.

supporting information, p. 1540 - 1543 (2014/03/21)

A simple synthetic procedure for the conversion of amines and hydrazines into substituted semicarbazides was developed. The initial condensation between the desired amine and phenyl chloroformate into phenyl carbamate is followed by the addition of hydrazine under basic conditions. The reaction is tolerable to a variety of functional groups, with mild conditions and high percent yields.

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