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

69380-84-3

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69380-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69380-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69380-84:
(7*6)+(6*9)+(5*3)+(4*8)+(3*0)+(2*8)+(1*4)=163
163 % 10 = 3
So 69380-84-3 is a valid CAS Registry Number.

69380-84-3SDS

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 4-methyl-N-propan-2-ylidenebenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-isopropylidene-4-methylbenzensulfonamide

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:69380-84-3 SDS

69380-84-3Relevant academic research and scientific papers

The first example of saccharin-lithium bromide catalysis: Direct synthesis of N-tosylimines from alcohols

Patel, Rajesh,Srivastava, Vishnu P.,Yadav, La Dhar S.

experimental part, p. 1610 - 1614 (2010/09/05)

The first procedure to access N-tosylimines directly from alcohols under mild and neutral conditions is reported. The protocol involves saccharin-lithium bromide-catalyzed oxidation of alcohols to aldehydes/ketones with chloramine-T followed by their condensation with the in situ generated oxidation by-product p-toluenesulfonamide in the same reaction vessel to afford N-tosylimines in 40-90% overall yields. The present work opens up a new and efficient synthetic route to N-tosyimines directly from alcohols in a one-pot procedure.

Gold catalysis: Switching the pathway of the furan-yne cyclization

Hashmi, A. Stephen K.,Rudolph, Matthias,Huck, Juergen,Frey, Wolfgang,Bats, Jan W.,Hamzic, Melissa

supporting information; experimental part, p. 5848 - 5852 (2009/12/06)

Changing tracks: By the use of alkynyl ethers as directing elements, the furan-yne cyclization enters a new reaction pathway. Instead of phenols, tetracycles containing two heteroatoms and two new stereocenters are formed (see scheme).

3,3-Disubstituted 2-Sulphonyloxaziridines: Synthesis and Observation of Isomeric Nitrogen Invertomers

Jennings, W. Brian,Watson, Stephen P.,Boyd, Derek R.

, p. 931 - 932 (2007/10/02)

The synthesis of the title compounds from oximes is described; some of these compounds provide the first reported examples of cis-trans isomerism in N-sulphonyloxaziridines.

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