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Benzenamine, 2,2'-dithiobis[N-[3-methyl-1-(2-methyl-2-propenyl)-3-butenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91258-36-5

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91258-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91258-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91258-36:
(7*9)+(6*1)+(5*2)+(4*5)+(3*8)+(2*3)+(1*6)=135
135 % 10 = 5
So 91258-36-5 is a valid CAS Registry Number.

91258-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-dithiodi-<N-(di-2-methyl-2-propenyl)methyl>aniline

1.2 Other means of identification

Product number -
Other names 2,2'-dithiodi-[N-(di-2-methyl-2-propenyl)methyl]aniline

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:91258-36-5 SDS

91258-36-5Downstream Products

91258-36-5Relevant academic research and scientific papers

RING OPENING OF BENZOTHIAZOLES WITH ALLYLIC GRIGNARD REAGENTS

Babudri, F.,Bartoli, G.,Ciminale, F.,Florio, S.,Ingrosso, G.

, p. 2047 - 2050 (2007/10/02)

A novel ring opening reaction of the benzothiazole system with allylic Grignard reagents is reported.A possible mechanism is presented.

REACTION OF 2-HETEROSUBSTITUTED BENZOTHIAZOLES WITH ALLYLIC GRIGNARD REAGENTS

Florio, Saverio,Epifani, Erbana,Ingrosso, Giovanni

, p. 4527 - 4534 (2007/10/02)

The title benzothiazoles 1 react with allylic Grignard reagents affording 2-allylbenzothiazoles 5, 2,2-diallylbenzothiazolines 6 and N-triallylmethyl-o-aminobenzenethiols as disulphides 7 depending upon the experimental conditions.The reaction is considerably influenced by the solvent used and the nature of the allylic Grignard.A possible mechanism for the formation of compounds 5, 6 and 7 is reported.

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