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2-Azetidinone, 4-(2-phenylethenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103564-07-4

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103564-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103564-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103564-07:
(8*1)+(7*0)+(6*3)+(5*5)+(4*6)+(3*4)+(2*0)+(1*7)=94
94 % 10 = 4
So 103564-07-4 is a valid CAS Registry Number.

103564-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trans-2-phenylethenyl)azetidin-2-one

1.2 Other means of identification

Product number -
Other names 4-E-styrylazetidinone

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:103564-07-4 SDS

103564-07-4Relevant academic research and scientific papers

SYNTHESIS OF β,γ-UNSATURATED AMIDES VIA PALLADIUM-PROMOTED COUPLING OF ORGANOMERCURIALS AND VINYLIC β-LACTAMS

Larock, Richard C.,Ding, Shuji

, p. 1897 - 1900 (2007/10/02)

The reaction of aryl or vinylic mercurials, Li2PdCl4 and vinylic β-lactams affords good yields of the corresponding ring-opened β,γ-unsaturated amides.

Synthesis and Ring Expansion of Vinylazetidines. A synthesis of Hydroazocines

Hassner, Alfred,Wiegand, Norbert

, p. 3652 - 3656 (2007/10/02)

A synthesis of 2-vinylazetidines 11a-c by means of ClSO2NCO addition to 1,3-dienes followed by AlH3 reduction is described.One example (11a) underwent Michael additions with several olefinic and acetylenic substrates.The 1,2-divinylazetidines obtained wit

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