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3-Pyridinemethanol,alpha-1,2-propadienyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

517907-47-0

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517907-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 517907-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,7,9,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 517907-47:
(8*5)+(7*1)+(6*7)+(5*9)+(4*0)+(3*7)+(2*4)+(1*7)=170
170 % 10 = 0
So 517907-47-0 is a valid CAS Registry Number.

517907-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (RS)-1-(3-pyridyl)buta-2,3-dien-1-ol

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:517907-47-0 SDS

517907-47-0Relevant academic research and scientific papers

Allenylic Carbonates in Enantioselective Iridium-Catalyzed Alkylations

Petrone, David A.,Isomura, Mayuko,Franzoni, Ivan,R?ssler, Simon L.,Carreira, Erick M.

supporting information, p. 4697 - 4704 (2018/04/11)

An enantioconvergent C(sp3)-C(sp3) coupling between racemic allenylic electrophiles and alkylzinc reagents has been developed. An Ir/(phosphoramidite,olefin) catalyst provides access to highly enantioenriched allenylic substitution p

Chemoenzymatic synthesis of optically active heterocyclic homoallylic and homopropargylic alcohols

Singh, Satwinder,Kumar, Subodh,Chimni, Swapandeep Singh

, p. 2679 - 2687 (2007/10/03)

A chemoenzymatic methodology has been developed using indium-mediated allylation of heterocyclic aldehydes under aqueous conditions followed by Pseudomonas cepacia lipase-catalyzed enantioselective acylation of racemic homoallylic and homopropargylic alcohols in organic media. It is observed that the lipase immobilized on ceramic particles (PS-C Amano II) catalyzes the resolution in a highly enantioselective manner in less time as compared to the native enzyme (PS Amano). The approach provides new functionalized chiral synthons useful in the synthesis of natural and pseudonatural products.

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