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α,α-Bis(trimethylsilyl)benzylalkohol is a complex organic compound with the molecular formula C14H26OSi2. It is characterized by a benzyl alcohol structure, where the hydroxyl group (-OH) is attached to a benzyl group. Unique to α,α-Bis(trimethylsilyl)benzylalkohol are the two trimethylsilyl groups (-Si(CH3)3) attached to the alpha carbons of the benzyl group, which are the carbons adjacent to the hydroxyl group. These silyl groups can protect the hydroxyl group from unwanted reactions, making α,α-Bis(trimethylsilyl)benzylalkohol a valuable intermediate in organic synthesis, particularly in the protection of alcohols. The compound is also known for its stability and is used in various chemical transformations where the hydroxyl group needs to be temporarily masked.

31129-63-2

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31129-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31129-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,2 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31129-63:
(7*3)+(6*1)+(5*1)+(4*2)+(3*9)+(2*6)+(1*3)=82
82 % 10 = 2
So 31129-63-2 is a valid CAS Registry Number.

31129-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α,α-Bis(trimethylsilyl)benzylalkohol

1.2 Other means of identification

Product number -
Other names Bis(trimethylsilyl)phenylmethanol

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:31129-63-2 SDS

31129-63-2Relevant academic research and scientific papers

Synthesis of bis(trimethylsilyl) ketone and reactions with organometallic compounds

Pan, Ming,Benneche, Tore

, p. 1141 - 1143 (2007/10/03)

Bis(trimethylsilyl) ketone (1) has been prepared by hydrolysis of the α-chloro ether 3a on silica gel. Reaction of ketone 1 with organoaluminium, organomagnesium and organolithium compounds gave addition products and/or bis(trimethylsilyl)methanol (5). Acta Chemica Scandinavica 1998.

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