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2-Pentynoic acid, 5-(1-cyclohexen-1-yl)-4-hydroxy-, methyl ester, (4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185397-10-8

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185397-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185397-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 185397-10:
(8*1)+(7*8)+(6*5)+(5*3)+(4*9)+(3*7)+(2*1)+(1*0)=168
168 % 10 = 8
So 185397-10-8 is a valid CAS Registry Number.

185397-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (4R)-5-(cyclohexen-1-yl)-4-hydroxypent-2-ynoate

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:185397-10-8 SDS

185397-10-8Relevant academic research and scientific papers

Regio- and enantioselective synthesis of allenic esters by samarium(II)-mediated reduction of propargylic compounds through dynamic kinetic protonation

Mikami, Koichi,Yoshida, Akihiro

, p. 889 - 898 (2001)

Regioselective synthesis of allenic esters was attained by SmI2-mediated reduction of propargylic phosphates and ethers bearing alkoxycarbonyl groups at the acetylene terminus. Using suitable chiral proton source in this system, highly enantio-

Catalytic asymmetric carbonyl-ene reactions with alkynylogous and vinylogous glyoxylates: Application to controlled synthesis of chiral isocarbacyclin analogues

Mikami, Koichi,Yoshida, Akihiro,Matsumoto, Youichi

, p. 8515 - 8518 (2007/10/03)

The asymmetric carbonyl-ene reaction with alkynylogous and vinylogous glyoxylates (1, 2) catalyzed by a binaphthol-derived chiral titanium complex is described. The catalytic asymmetric ene reaction with aldehyde (1) can be applied to the double asymmetric synthesis of isocarbacyclin analogues bearing a 2-allenyl side chain.

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