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614-63-1

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614-63-1 Usage

Chemical Class

The compound belongs to the triazene class of organic compounds.

Structure

The compound has two methylphenyl groups attached to a central triazene group.

Synthesis

The compound is commonly used in the synthesis of various organic compounds.

Versatility

The compound is versatile and has potential use in pharmaceuticals, dyes, and other chemical applications.

Properties and Uses

The exact properties and uses of 1-Triazene, 1,3-bis(2-methylphenyl)depend on its specific applications and can vary widely in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 614-63-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 614-63:
(5*6)+(4*1)+(3*4)+(2*6)+(1*3)=61
61 % 10 = 1
So 614-63-1 is a valid CAS Registry Number.

614-63-1SDS

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 1,3-di-o-tolyltriazene

1.2 Other means of identification

Product number -
Other names 1-Triazene, 1,3-bis(2-methylphenyl)-

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:614-63-1 SDS

614-63-1Upstream product

614-63-1Relevant articles and documents

Synthesis and properties of amphiphilic photoresponsive gelators for aromatic solvents

Rajaganesh, Ramanathan,Gopal, Anesh,Mohan Das, Thangamuthu,Ajayaghosh, Ayyappanpillai

supporting information; experimental part, p. 748 - 751 (2012/03/26)

A sugar-based photoresponsive supergelator, N-glycosylazobenzene that shows selective gelation of aromatic solvents is described. The partial trans - cis isomerization of the azobenzene moiety allows photoinduced chopping of the entangled gel fibers to short fibers, resulting in controlled fiber length and gel - sol transition. The gelator is useful for the selective removal of toxic aromatic solvents from water.

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