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Benzenesulfonamide, 4-methyl-N-(3-phenyl-4,5-hexadienyl)-, also known as 4-Methyl-N-(3-phenyl-4,5-hexadienyl)benzenesulfonamide, is a chemical compound with the molecular formula C15H17NO2S. It is a derivative of benzenesulfonamide, featuring a 4-methyl group and a 3-phenyl-4,5-hexadienyl moiety attached to the nitrogen atom. Benzenesulfonamide, 4-methyl-N-(3-phenyl-4,5-hexadienyl)- is characterized by its yellowish color and is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. The compound's properties, such as its solubility and stability, make it a valuable intermediate in the production of certain drugs and pesticides.

137401-51-5

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137401-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137401-51-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137401-51:
(8*1)+(7*3)+(6*7)+(5*4)+(4*0)+(3*1)+(2*5)+(1*1)=105
105 % 10 = 5
So 137401-51-5 is a valid CAS Registry Number.

137401-51-5SDS

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 4-methyl-N-(3-phenylhexa-4,5-dienyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonamide,4-methyl-N-(3-phenyl-4,5-hexadienyl)

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:137401-51-5 SDS

137401-51-5Relevant academic research and scientific papers

Ring opening of 2-phenylazetidines with allylsilanes

Domostoj, Mathias,Ungureanu, Ioana,Schoenfelder, Angèle,Klotz, Philippe,Mann, André

, p. 2205 - 2208 (2007/10/03)

N-Activated 2-phenylazetidines were opened regioselectively at the benzylic carbon with various allylsilanes or propargylsilane in the presence of BF 3?Et2O, providing amino olefins, precursors of biomolecules such as phenyl-homo-kai

Stereoselectivity in Electrophile-Mediated Cyclisations. AgI-Catalysed Synthesis of Disubstituted Pyrrolidines; Crystal Structure of cis-5-Phenyl-N-tosylpyrrolidin-2-ylmethyl 4-Bromobenzoate

Gallagher, Timothy,Jones, Stephen W.,Mahon, Mary F.,Molloy, Kieran C.

, p. 2193 - 2198 (2007/10/02)

A series of phenyl-substituted allenic sulphonamides 5, 6 and 7 have been prepared and shown to undergo AgI-catalysed cyclisation to give the corresponding 2,5-, 2,4- and 2,3-disubstituted N-sulphonylpyrrolidines 8, 9, and 10 respectively.The i

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