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154557-38-7

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154557-38-7 Usage

Function

Silylating reagent in organic synthesis

Purpose

Protect hydroxyl groups in chemical reactions

Physical state

Colorless liquid at room temperature

Boiling point

159-161°C

Solubility

Soluble in organic solvents (e.g., ether, chloroform)

Stability

Stable under normal conditions

Application

Preparation of trimethylsilyl ethers

Utility

Useful tool in synthetic organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 154557-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,5,5 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 154557-38:
(8*1)+(7*5)+(6*4)+(5*5)+(4*5)+(3*7)+(2*3)+(1*8)=147
147 % 10 = 7
So 154557-38-7 is a valid CAS Registry Number.

154557-38-7SDS

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 trimethyl-(1-trimethylsilyl-3-trimethylsilyloxypropan-2-yl)oxysilane

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:154557-38-7 SDS

154557-38-7Downstream Products

154557-38-7Relevant articles and documents

The protection of ketones and aldehydes as 4-trimethylsilylmethyl-1,3- dioxolanes

Lillie,Avery

, p. 969 - 972 (1994)

The 1,3-dioxolanation of carbonyl compounds with 2,3- bis(trimethylsilyloxy)-trimethylsilylpropane (BTTP) in the presence of catalytic amounts of trimethylsilyl trifluoromethanesulfonate (TMSOTf) has been investigated. BTTP readily converted unhindered ketones and aldehydes to their corresponding 4-trimethylsilylmethyl-1,3-dioxolanes, but failed for more hindered substrates. The 4-trimethylsilylmethyl-1,3-dioxolane can be selectively cleaved to regenerate the carbonyl compound in the presence of a 1,3-dioxolane using either LiBF4 or HF in acetonitrile.

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