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(2E)-3-(1,3-benzodioxol-5-yl)-N-[2-(benzylsulfanyl)ethyl]prop-2-enamide is a complex organic compound with a molecular formula of C20H19NO3S. It features a 2-eneamide backbone, with a 1,3-benzodioxol-5-yl group attached at the 3-position and a benzylsulfanylethyl group at the nitrogen atom. (2E)-3-(1,3-benzodioxol-5-yl)-N-[2-(benzylsulfanyl)ethyl]prop-2-enamide is characterized by its unique structure, which includes a benzodioxole ring, a prop-2-enamide group, and a benzylsulfanylethyl moiety. It is likely to have specific chemical properties and reactivity due to the presence of these functional groups, and may be of interest in the fields of organic chemistry, pharmaceuticals, or materials science for its potential applications or as a building block in the synthesis of more complex molecules.

6401-46-3

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6401-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6401-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6401-46:
(6*6)+(5*4)+(4*0)+(3*1)+(2*4)+(1*6)=73
73 % 10 = 3
So 6401-46-3 is a valid CAS Registry Number.

6401-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(1,3-benzodioxol-5-yl)-N-(2-benzylsulfanylethyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names -

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:6401-46-3 SDS

6401-46-3Downstream Products

6401-46-3Relevant academic research and scientific papers

PH-Dependent peptide bond formation by the selective coupling of α-amino acids in water

Wu, Long-Fei,Liu, Ziwei,Sutherland, John D.

supporting information, p. 73 - 76 (2021/01/13)

A novel mechanism enabling selective peptide elongation by coupling α-amino acids over other potentially competing prebiotic amines under acidic aqueous condition is suggested. It proceeds via the generation of a carboxylic acid anhydride intermediate with subsequent intramolecular formation of the amide bond. This journal is

Peptide ligation by chemoselective aminonitrile coupling in water

Canavelli, Pierre,Islam, Saidul,Powner, Matthew W.

, p. 546 - 549 (2019/07/31)

Amide bond formation is one of the most important reactions in both chemistry and biology1–4, but there is currently no chemical method of achieving α-peptide ligation in water that tolerates all of the 20 proteinogenic amino acids at the pepti

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