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1,2,4,5-Tetrazine, 3-(4-chlorophenyl)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56107-76-7

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56107-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56107-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,0 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56107-76:
(7*5)+(6*6)+(5*1)+(4*0)+(3*7)+(2*7)+(1*6)=117
117 % 10 = 7
So 56107-76-7 is a valid CAS Registry Number.

56107-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)-6-methyl-1,2,4,5-tetrazine

1.2 Other means of identification

Product number -
Other names -

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:56107-76-7 SDS

56107-76-7Relevant academic research and scientific papers

REAGENTS AND METHODS FOR TETRAZINE SYNTHESIS

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Paragraph 0139-0143; 0146; 0147, (2022/04/09)

Disclosed herein are mono- and di-substituted tetrazines and methods of their preparation and converting an oxetanyl ester to a thio-substituted tetrazine, which is then converted to a mono-substituted tetrazine, a di-substituted tetrazine, or a vinylether disubstituted tetrazine.

Synthesis, structures of some unsymmetrical 3,6-disubstituted-1,2,4,5- tetrazines

Hu, Wei-Xiao,Xu, Feng

experimental part, p. 1745 - 1750 (2009/05/31)

(Chemical Equation Presented) A series of new unsymmetrical 3-phenyl-6-benzyl-1,2,4,5-tetrazine derivatives 10a-i were synthesized and characterized by IR, NMR, MS, and element analysis. The structures of 4a, 10c, 10d and 10h were analyzed by X-ray crystallography, which had intermolecular C-H...N, C-H...Cl, C-H...Π and Π...Π H interactions.

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