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672-25-3

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672-25-3 Usage

General Description

(Aminomethylene)malononitrile is a chemical compound with the molecular formula C4H2N4. It is a highly reactive and versatile intermediate that is commonly used in organic synthesis for the production of various functional compounds. (aminomethylene)malononitrile is a key building block for the preparation of heterocyclic structures and has been utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique structure and reactivity, (aminomethylene)malononitrile has garnered significant interest in the field of organic chemistry and has been the subject of numerous research studies and applications. Its ability to undergo various chemical transformations makes it a valuable tool for the development of new products and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 672-25-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 672-25:
(5*6)+(4*7)+(3*2)+(2*2)+(1*5)=73
73 % 10 = 3
So 672-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H3N3/c5-1-4(2-6)3-7/h1H,5H2

672-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aminomethylidene)propanedinitrile

1.2 Other means of identification

Product number -
Other names 2-Aminomethylenepropanedinitrile

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:672-25-3 SDS

672-25-3Relevant articles and documents

Oxidative peptide bond formation of glycine-amino acid using 2-(aminomethyl)malononitrile as a glycine unit

Wang, Xiaoling,Li, Jing,Hayashi, Yujiro

supporting information, p. 4283 - 4286 (2021/05/05)

Amide linkage of glycine-amino acid was synthesized by coupling of substituted 2-(aminomethyl)malononitrile as a C-terminal glycine unit and N-terminal amine using CsOAc and O2in an aqueous solution. This is a coupling reagent-free and catalyst-free peptide synthesisviaoxidative amide bond formation. Various tripeptides and tetrapeptides were synthesized efficiently and the sulfide moiety is inert even under an oxygen atmosphere.

Studies on pyrimidine derivatives. VIII. Ring-cleavage reaction of 4,6-dimethylpyrimidine 1-oxide

Yamanaka,Sakamoto,Bannai,Ogawa

, p. 3404 - 3409 (2007/10/04)

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