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Trimethyl-(1-phenyl-buta-2,3-dienyloxy)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108164-63-2

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108164-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108164-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,6 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108164-63:
(8*1)+(7*0)+(6*8)+(5*1)+(4*6)+(3*4)+(2*6)+(1*3)=112
112 % 10 = 2
So 108164-63-2 is a valid CAS Registry Number.

108164-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl((1-phenylbuta-2,3-dien-1-yl)oxy)silane

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:108164-63-2 SDS

108164-63-2Downstream Products

108164-63-2Relevant academic research and scientific papers

Studies on catalytic asymmetric Nozaki-Hiyama propargylation

Inoue, Masahiro,Nakada, Masahisa

, p. 2977 - 2980 (2007/10/03)

(Equation Presented) Catalytic asymmetric Nozaki-Hiyama propargylation with ligand 1c proceeds with good to excellent enantioselectivity. Tuning of ligand 1 dramatically changes the enantioselectivity, and we propose models A and B to explain the change a

Lead Promoted Barbier-Type Reaction of Propargyl Bromide with Aldehydes

Tanaka, Hideo,Hamatani, Takeshi,Yamashita, Shiro,Torii, Sigeru

, p. 1461 - 1462 (2007/10/02)

The first example of lead promoted "Barbier-type" (in situ Grignard) reaction has been demonstrated by the reaction of propargyl bromide with aldehydes in a Pb/Bu4NBr/Me3SiCl/DMF system.

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