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51384-73-7

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51384-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51384-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,8 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51384-73:
(7*5)+(6*1)+(5*3)+(4*8)+(3*4)+(2*7)+(1*3)=117
117 % 10 = 7
So 51384-73-7 is a valid CAS Registry Number.

51384-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylpent-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3-Penten-2-one,4-phenyl

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:51384-73-7 SDS

51384-73-7Relevant articles and documents

Lewis Acid Catalyzed Ring-Opening Reaction of Cyclobutanones towards Conjugated Enones

Gao, Jiqiang,Guo, Ziteng,Li, Zhongjuan,Liu, Chunhui,Liu, Yu,Qiu, Tingtian,Zhang, Min,Zhao, Jinbo

, p. 6111 - 6114 (2021/12/16)

An unprecedented Fe-catalyzed ring-opening reaction of simple cyclobutanones is developed, which provides access to conjugated enones with good functional group tolerance in high yields under mild conditions. The product derivatization and gram-scale expe

Rearrangement Reactions Leading to Optically Active α,α-Disubstituted Primary Allylamines

Hennum, Martin,Odden, Hege Hortemo,Gundersen, Lise-Lotte

, p. 846 - 860 (2017/02/15)

Synthetic routes to α,α-disubstituted allylamines have been examined. Racemic compounds were conveniently prepared by thermal Overman rearrangements of primary allylic alcohols with trisubstituted double bonds, but rearrangement of these substrates using

Catalytic stereospecific allyl-allyl cross-coupling of internal allyl electrophiles with allylB(pin)

Le, Hai,Batten, Amanda,Morken, James P.

supporting information, p. 2096 - 2099 (2014/05/06)

Application of internal electrophiles in catalytic stereospecific allyl-allyl cross-coupling enable the rapid construction of multisubstituted 1,5-dienes, including those with all carbon quaternary centers. Compounds with minimal steric differentiation ca

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