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2,2',4,4'-Tetrabutyl-6,6'-dimethylazobenzene is an organic compound characterized by its azobenzene structure, which features a nitrogen-nitrogen double bond connecting two aromatic rings. This particular compound is distinguished by the presence of four butyl groups (each consisting of a four-carbon chain) and two methyl groups (each consisting of a single carbon) attached to the benzene rings. It is known for its potential applications in various fields, such as in the synthesis of dyes and as a component in certain chemical reactions. Due to its complex structure, it is important to handle 2,2',4,4'-Tetrabutyl-6,6'-dimethylazobenzene with care, adhering to proper safety protocols to minimize any potential health or environmental risks.

35532-72-0

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35532-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35532-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,3 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35532-72:
(7*3)+(6*5)+(5*5)+(4*3)+(3*2)+(2*7)+(1*2)=110
110 % 10 = 0
So 35532-72-0 is a valid CAS Registry Number.

35532-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2',4,4'-tetra-t-butyl-6,6'-dimethylazobenzene

1.2 Other means of identification

Product number -
Other names 2,2',4,4'-Tetra-tert-butyl-6,6'-dimethyl-azobenzol

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:35532-72-0 SDS

35532-72-0Downstream Products

35532-72-0Relevant academic research and scientific papers

Chemistry of N-Thiosulfinylanilines. V. Reactions of N-Thiosulfinylanilines with Nucleophilic Reagents

Inagaki, Yoshio,Hosogai, Takeo,Okazaki, Renji,Inamoto, Naoki

, p. 205 - 209 (2007/10/02)

2,4-Di-t-butyl-6-methyl-N-(thiosulfinyl)aniline (1) gave 2,4-di-t-butyl-6-methylaniline in the reactions with such reagents as alkylamines, thiourea, butyllithium, alkylmagnesium halides, 1-(1-pyrrolidinyl)cyclopentene, and hydrogen sulfide.Triphenylphosphine reacted with 1 to give (2,4-di-t-butyl-6-methylphenylimino)triphenylphosphorane and bis(2,4-di-t-butyl-6-methylphenyl)sulfur diimide.Reaction of triphenylphosphine with 2,4,6-tri-t-butyl-7,8-dithia-9-azabicyclonona-2,4,9-triene afforded 2,4,6-tri-t-butylaniline, bis(2,4,6-tri-t-butylphenyl)sulfur diimide, and 2,4,6-tri-t-butyl-N-sulfinylaniline (7).The sulfur diimide was considered to be formed via intermediary 2,4,6-tri-t-butylthionitrosobenzene, which was trapped by oxygen to give the N-sulfinyl derivative 7.

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