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3-Pyridinemethanol, a-cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70423-46-0

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70423-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70423-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,2 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70423-46:
(7*7)+(6*0)+(5*4)+(4*2)+(3*3)+(2*4)+(1*6)=100
100 % 10 = 0
So 70423-46-0 is a valid CAS Registry Number.

70423-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Cyclohexyl-3-pyridinmethanol

1.2 Other means of identification

Product number -
Other names Cyclohexyl-3-pyridylmethanol

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:70423-46-0 SDS

70423-46-0Relevant academic research and scientific papers

Copper-dipyridylphosphine-catalyzed hydrosilylation: Enantioselective synthesis of aryl- and heteroaryl cycloalkyl alcohols

Qi, Shan-Bin,Li, Min,Li, Shijun,Zhou, Ji-Ning,Wu, Jun-Wen,Yu, Feng,Zhang, Xi-Chang,Chan, Albert S.C.,Wu, Jing

, p. 929 - 937 (2013/02/26)

The non-precious metal copper-catalyzed enantioselective hydrosilylation of a vast array of aryl cycloalkyl ketones with different ring sizes was studied systematically for the first time (up to 99% enantiomeric excess). The results demonstrated that the

Fungicidal Pyridine Derivatives I: α-Trichloromethyl-3-pyridinemethanols

Sauter, Fritz,Stanetty, Peter,Sittenthaler, Wilhelm,Waditschatka, Rudolf

, p. 1427 - 1438 (2007/10/02)

The title substances, a new type of compounds with fungicidal activity, were synthesized by addition of trichloromethyllithium (and tribromomethyllithium resp.) to various 3-pyridyl ketones at -100 deg C. - Keywords: Fungicides; Pyridinemethanoles; Trichl

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