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2-Propenoic acid, (1R)-1-(2-phenylethyl)-3-butenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

350482-51-8

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350482-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350482-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,4,8 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 350482-51:
(8*3)+(7*5)+(6*0)+(5*4)+(4*8)+(3*2)+(2*5)+(1*1)=128
128 % 10 = 8
So 350482-51-8 is a valid CAS Registry Number.

350482-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3R)-1-phenylhex-5-en-3-yl] prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,(1R)-1-(2-phenylethyl)-3-butenyl ester

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:350482-51-8 SDS

350482-51-8Relevant academic research and scientific papers

Cytotoxic activity of (S)-goniothalamin and analogues against human cancer cells

De Fatima, Angelo,Kohn, Luciana K.,De Carvalho, Joao Ernesto,Pilli, Ronaldo A.

, p. 622 - 631 (2007/10/03)

(R)- and (S)-Goniothalamin (1) and analogues 2-9 were efficiently prepared in high overall yield and enantiomeric purity, and their cytotoxic activities were evaluated against eight human cancer cell lines. A structure-activity relationship study (SAR) al

Asymmetric allylboration for the synthesis of β-hydroxy-δ-lactone unit of statin drug analogs

Reddy, M. Venkat Ram,Brown, Herbert C.,Ramachandran, P. Veeraraghavan

, p. 239 - 243 (2007/10/03)

Acrylic esters of homoallylic alcohols prepared in 92-96% ee via the asymmetric allylboration of appropriate aldehydes with B-allyldiisopinocampheylborane, upon ring-closing metathesis in the presence of 10mol% of Grabbs' catalyst provided the correspondi

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