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2-Propenamide, N-ethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23784-45-4

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23784-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23784-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,8 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23784-45:
(7*2)+(6*3)+(5*7)+(4*8)+(3*4)+(2*4)+(1*5)=124
124 % 10 = 4
So 23784-45-4 is a valid CAS Registry Number.

23784-45-4SDS

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-ethyl-cinnamamide

1.2 Other means of identification

Product number -
Other names N-Aethyl-cinnamamid

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:23784-45-4 SDS

23784-45-4Relevant academic research and scientific papers

Generation of alkyl radicals from alkylsilyl peroxides and their applications to C-N or C-O bond formations

Sakurai, Shunya,Kato, Terumasa,Sakamoto, Ryu,Maruoka, Keiji

, p. 172 - 179 (2018/12/11)

This article describes a novel method for the generation of alkyl radicals from alkylsilyl peroxides and their applications to the Cu-catalyzed mono-N-alkylation of amides or arylamines, and to the O-alkylation of carboxylic acids. The use of alkylsilyl peroxides as alkyl radical sources includes the following synthetic advantages: i) various alkylsilyl peroxides can be readily synthesized from the corresponding alcohols and be stored at bench, and ii) a variety of alkyl radicals can be generated efficiently under mild conditions.

INTRAMOLECULAR RADICAL TRAPPING IN "SET" RING OPENING OF N-ENOYL AZIRIDINES. A NEW MECHANISTIC PROBE AND A NEW SYNTESIS OF PYRROLIDONES.

Bentz, G.,Besbes, N.,Laurent, A.,Stamm, H.

, p. 2511 - 2512 (2007/10/02)

N-Acryloyl aziridines 1a-c form pyrrolidones 4a-c via electron attachment, homolytic ring cleavage of the intermediate ketyl, and intramolecular trapping of the radical by the C=C bond of the acryloyl moiety of 1a-c.

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