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Silane, cyclohexylmethylphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64358-63-0

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64358-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64358-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,5 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64358-63:
(7*6)+(6*4)+(5*3)+(4*5)+(3*8)+(2*6)+(1*3)=140
140 % 10 = 0
So 64358-63-0 is a valid CAS Registry Number.

64358-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylmethyl(phenyl)silane

1.2 Other means of identification

Product number -
Other names cyclohexylphenylmethylsilane

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:64358-63-0 SDS

64358-63-0Relevant academic research and scientific papers

Selective synthesis of monohydrosilanes by the reactions of organoytterbium iodides with dihydrosilanes

Jin, Wu-Song,Makioka, Yoshikazu,Kitamura, Tsugio,Fujiwara, Yuzo

, p. 955 - 956 (2007/10/03)

Monohydrosilanes can be prepared selectively in high yields from the reaction of various aryl and alkyl iodides with ytterbium metal followed by the reaction with dihydrosilanes.

Sila-Pharmaca, 36. - Sila-Procyclidine: A New Synthesis as well as Investigations of the Peripheral and Central Anticholinergic Activity

Tacke, Reinhold,Pikies, Jerzy,Linoh, Haryanto,Rohr-Aehle, Regine,Goenne, Sigrid

, p. 51 - 58 (2007/10/02)

Starting with Cl3SiCH2Cl, sila-procyclidine (1b) as well as its derivatives 2b (sila-trihexyphenidyl), 3b, and 4b (sila-cycrimine) were prepared by a new six-step synthesis with a total yields of 16 (1b), 19 (2b), 8 (3b) and 7percent (4b), respectively. -

ASYMMETRIC INDUCTION BY CHIRAL SILICON GROUPS

Larson, Gerald L.,Torres, Evelyn

, p. 19 - 28 (2007/10/02)

The reduction of racemic RPhMeSiCCl2CH3 systems (R=cyclohexyl, isoprpyl, t-butyl and 2-mesityl) to the diastereomeric RPhMeSiCHClCH3 with tributyltin hydride was used as a probe into the potential of the RPhMeSi group to induce asymmetry at an α position.Favorable results were obtained for R=mesityl.

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