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4-Hexen-2-ol, 1-(phenylmethoxy)-, (2R,4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115560-90-2

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115560-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115560-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,6 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115560-90:
(8*1)+(7*1)+(6*5)+(5*5)+(4*6)+(3*0)+(2*9)+(1*0)=112
112 % 10 = 2
So 115560-90-2 is a valid CAS Registry Number.

115560-90-2SDS

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 (2R)-(E)-1-(phenylmethoxy)-4-hexen-2-ol

1.2 Other means of identification

Product number -
Other names (R,E)-1-(benzyloxy)hex-4-en-2-ol

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:115560-90-2 SDS

115560-90-2Relevant academic research and scientific papers

Heteroaryl-Substituted Hexahydropyrano[3,4-d][1,3]Thiazin-2-Amine Compounds

-

, (2014/08/19)

The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, and the variables R1 and R2 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

Highly (E)-selective BF3·Et2O-promoted allylboration of chiral nonracemic α-Substituted allylboronates and analysis of the origin of stereocontrol

Chen, Ming,Roush, William R.

supporting information; experimental part, p. 2706 - 2709 (2010/11/18)

(Figure presented) δ-Methyl-substituted homoallylic alcohols 2 were prepared in 71-88% yield, E:Z >30:1 and 93% to >95% ee via BF 3·Et2O-promoted allylboration with α-Me-allylboronate 1. The origin of high (E)-selectivity is proposed

A convergent route to β-hydroxy δ-lactones through Prins cyclisation as the key step: Synthesis of (+)-prelactones B, C and V

Yadav,Reddy, M. Sridhar,Prasad

, p. 2133 - 2136 (2007/10/03)

Reactions of homoallylic alcohols with aldehydes in the presence of acid catalysts gave multisubstituted tetrahydropyrans with the creation of one to three new stereogenic centres in a single-pot process. The utility of this approach is extended to the en

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