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Benzenesulfonamide, N,4-dimethyl-N-(1-methyl-2-butenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106003-87-6

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106003-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106003-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,0 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106003-87:
(8*1)+(7*0)+(6*6)+(5*0)+(4*0)+(3*3)+(2*8)+(1*7)=76
76 % 10 = 6
So 106003-87-6 is a valid CAS Registry Number.

106003-87-6SDS

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 N-methyl-N'-(1-methyl-2-butenyl)-p-toluenesulfamide

1.2 Other means of identification

Product number -
Other names 4,N-Dimethyl-N-((E)-1-methyl-but-2-enyl)-benzenesulfonamide

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:106003-87-6 SDS

106003-87-6Downstream Products

106003-87-6Relevant academic research and scientific papers

1,1′-(azodicarbonyl)dipiperidine-tributylphosphine, a new reagent system for mitsunobu reaction

Tsunoda, Tetsuto,Yamamiya, Yoshiko,Ito, Sho

, p. 1639 - 1642 (2007/10/02)

The 1,1′-(azodicarbonyl)dipiperidine (ADDP)-tributylphosphine (TBP) system was developed as a new institute of the Mitsunobu reagent. The new system activates nitrogen or carbon nucleophiles, known to be innert or poorly reactive with the Mitsunobu reagent, to react with alcohols satisfactorily forming C-N or C-C bonds. The inversion of stereogenic carbinyl carbons was confirmed in the acylaltion reaction of two sec-alcohols.

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