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3,5-Cyclohexadiene-1,2-diimine, 4-methyl-, also known as 4-methyl-1,2-diimino-3,5-cyclohexadiene, is an organic compound with the chemical formula C7H10N2. It is a derivative of cyclohexadiene, featuring two imine groups (-NH-) at the 1 and 2 positions, and a methyl group (-CH3) at the 4 position. 3,5-Cyclohexadiene-1,2-diimine, 4-methyl- is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its potential applications in the production of dyes and pigments. Due to its reactivity, it is typically handled under controlled conditions to prevent unwanted side reactions.

4377-72-4

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4377-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4377-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4377-72:
(6*4)+(5*3)+(4*7)+(3*7)+(2*7)+(1*2)=104
104 % 10 = 4
So 4377-72-4 is a valid CAS Registry Number.

4377-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(λ<sup>2</sup>-azanyl)-4-methylbenzene

1.2 Other means of identification

Product number -
Other names 3,5-Cyclohexadiene-1,2-diimine,4-methyl

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:4377-72-4 SDS

4377-72-4Downstream Products

4377-72-4Relevant academic research and scientific papers

Kinetic characterisation of o-aminophenols and aromatic o-diamines as suicide substrates of tyrosinase

Munoz-Munoz, Jose Luis,Garcia-Molina, Francisco,Berna, Jose,Garcia-Ruiz, Pedro Antonio,Varon, Ramon,Tudela, Jose,Rodriguez-Lopez, Jose N.,Garcia-Canovas, Francisco

experimental part, p. 647 - 655 (2012/08/08)

We study the suicide inactivation of tyrosinase acting on o-aminophenols and aromatic o-diamines and compare the results with those obtained for the corresponding o-diphenols. The catalytic constants follow the order aromatic o-diamines max/KmS, follows this order: o-diphenols > o-aminophenols > aromatic o-diamines.

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