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98603-79-3

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98603-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98603-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98603-79:
(7*9)+(6*8)+(5*6)+(4*0)+(3*3)+(2*7)+(1*9)=173
173 % 10 = 3
So 98603-79-3 is a valid CAS Registry Number.

98603-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [cyclopropyl(phenyl)methoxy]-trimethylsilane

1.2 Other means of identification

Product number -
Other names (cyclopropylphenylmethoxy)trimethylsilane

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:98603-79-3 SDS

98603-79-3Relevant articles and documents

Cross-linked poly(4-vinylpyridine/styrene) copolymer-supported bismuth(III) triflate: An efficient heterogeneous catalyst for silylation of alcohols and phenols with HMDS

Lee, Sang-Hyeup,Kadam, Santosh T.

experimental part, p. 608 - 615 (2011/11/12)

Cross-linked poly(4-vinylpyridine/styrene) copolymer-supported bismuth(III) triflate (30P/S-Bi) effectively activates hexamethyldisilazane (HMDS) for the silylation of alcohols and phenols. By the use of this heterogeneous catalytic system, a wide range of alcohols as well as phenols are converted into their corresponding trimethylsilyl ethers in high yield under mild reaction conditions. The catalyst was reused more than 10 times without significant loss of its catalytic activity.

Mild and efficient silylation of alcohols and phenols with HMDS using Bi(OTf)3 under solvent-free condition

Kadam, Santosh T.,Kim, Sung Soo

experimental part, p. 2562 - 2566 (2009/12/24)

A very efficient and mild silylation of alcohols and phenols with hexamethyldisilazane (HMDS) at rt is developed using Bi(OTf)3 as the catalyst. Primary, secondary and tertiary alcohols as well as phenols are excellently converted into correspo

A Novel Mechanism for the Conversion of α-Cyclopropylbenzyl Alcohol into γ-Trimethylsilylbutyrophenone

Hwu, Jih Ru

, p. 452 - 453 (2007/10/02)

Mechanistic studies of the reaction between α-cyclopropylbenzyl alcohol and methyl-lithium followed by hexamethyldisilane indicate that disproportionation of intermediate (4) with trimethylsilyl anion as catalyst provides cyclopropyl phenyl ketone; in situ 1,4-addition of trimethylsilyl anion to the latter compound leads to the major product, γ-trimethylsilylbutyrophenone (2).

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