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2917-40-0

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2917-40-0 Usage

General Description

4-(Trimethylsilyl)butan-1-ol is a chemical compound with the molecular formula C7H18OSi. It is a clear, colorless liquid that is commonly used as a reagent in organic synthesis and as a protective group for alcohols in organic chemistry reactions. It is also known as TBS-protected alcohol. 4-(TriMethylsilyl)butan-1-ol is derived from butanol and contains a trimethylsilyl group, which is often used to protect alcohols from unwanted reactions during chemical processes. It has a wide range of applications in the pharmaceutical and chemical industries, particularly in the synthesis of complex organic molecules. Additionally, it is often used in the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 2917-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2917-40:
(6*2)+(5*9)+(4*1)+(3*7)+(2*4)+(1*0)=90
90 % 10 = 0
So 2917-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H18OSi/c1-9(2,3)7-5-4-6-8/h8H,4-7H2,1-3H3

2917-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-trimethylsilylbutan-1-ol

1.2 Other means of identification

Product number -
Other names 4-trimethylsilanyl-butan-1-ol

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:2917-40-0 SDS

2917-40-0Relevant articles and documents

One-Pot Conversions of (Silylmethyl)cyclopropanes to Homoallylic Alcohols and 1,4-Diols Based on Haloborane-Induced Ring Opening

Ryu, Ilhyong,Hirai, Akira,Suzuki, Haruhisa,Sonoda, Noboru,Murai, Shinji

, p. 1409 - 1410 (2007/10/02)

The reactions of (silylmethyl)cyclopropanes with haloboranes, such as BBr3 and BHBr2, result in desilylative ring opening to give homoallylboranes and boracyclopentanes, respectively.Coupled with subsequent oxidation procedure, these reactions provide ready access to homoallylic alcohols and 1,4-diols.

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