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2-Butenoic acid, 4-(acetyloxy)-3-phenyl-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72335-13-8

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72335-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72335-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72335-13:
(7*7)+(6*2)+(5*3)+(4*3)+(3*5)+(2*1)+(1*3)=108
108 % 10 = 8
So 72335-13-8 is a valid CAS Registry Number.

72335-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-Ethyl 4-Acetoxy-3-phenylbut-2-enecarboxylate

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:72335-13-8 SDS

72335-13-8Relevant academic research and scientific papers

Synthetic Approaches to the Naphthyl-isoquinoline Alkaloids. Part 2. The Total Synthesis of (-)-O-Methylancistrocladine and (+)-O-Methylhamatine and their Enantiomers

Rizzacasa, Mark A.,Sargent, Melvyn V.

, p. 845 - 854 (2007/10/02)

An asymmetric total synthesis of the naphthyl-isoquinoline alkaloids (-)-O-methylancistrocladine 39 is described; the synthetic method also provides routes to the atropisomer (+)-O-methylhamatine 43 and the enantiomers of these alkaloids.The asymmetric co

Resolved Monophenolic 2-Aminotetralins and 1,2,3,4,4a,5,6,10b-Octahydrobenzoquinolines: Structural and Stereochemical Cosiderations for Centrally Acting Pre- and Postsynaptic Dopamine-Receptor Agonists

Wikstroem, Hakan,Andersson, Bengt,Sanchez, Domingo,Lindberg, Per,Arvidsson, Lars-Erik,et al.

, p. 215 - 225 (2007/10/02)

A detailed structure-activity relationship is revealed for resolved, centrally acting dopamine (DA) agonists acting on both pre- and postsynaptic DA receptors.The compounds resolved are 5- and 7-hydroxy-2-(di-n-propylamino)tetralin and cis- and trans-7-hy

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