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Benzenemethanol, 2-fluoro-alpha-2-propynyl-, (alphaR)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

355806-87-0

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355806-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355806-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,8,0 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 355806-87:
(8*3)+(7*5)+(6*5)+(5*8)+(4*0)+(3*6)+(2*8)+(1*7)=170
170 % 10 = 0
So 355806-87-0 is a valid CAS Registry Number.

355806-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-(2-fluorophenyl)-3-butyn-1-ol

1.2 Other means of identification

Product number -
Other names Benzenemethanol, 2-fluoro-alpha-2-propynyl-, (alphaR)-

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:355806-87-0 SDS

355806-87-0Downstream Products

355806-87-0Relevant academic research and scientific papers

Optimization of Catalyst Structure for Asymmetric Propargylation of Aldehydes with Allenyltrichlorosilane

Vaganov, Vladimir Yu.,Fukazawa, Yasuaki,Kondratyev, Nikolay S.,Shipilovskikh, Sergei A.,Wheeler, Steven E.,Rubtsov, Aleksandr E.,Malkov, Andrei V.

supporting information, p. 5467 - 5474 (2020/10/19)

The design of catalysts for asymmetric propargylations remains a challenging task, with only a handful of methods providing access to enantioenriched homopropargylic alcohols. In this work, guided by previously reported computational predictions, a set of

Asymmetric nozaki-hiyama propargylation of aldehydes: Enhancement of enantioselectivity by cobalt co-catalysis

Usanov, Dmitry L.,Yamamoto, Hisashi

supporting information; experimental part, p. 8169 - 8172 (2011/02/24)

It takes two to tango! A combination of partially reduced chiral H 8-TBOx chromium catalyst 1 and achiral cobalt porphine co-catalyst 2 (Ar=p-anisyl) led to an enhancement in enantioselectivity by suppression of the background process that presumably proceeds through an organomanganese species.

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