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Benzoyl chloride, 2-[(trimethylsilyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79302-18-4

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79302-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79302-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79302-18:
(7*7)+(6*9)+(5*3)+(4*0)+(3*2)+(2*1)+(1*8)=134
134 % 10 = 4
So 79302-18-4 is a valid CAS Registry Number.

79302-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trimethylsiloxy)benzoyl chloride

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:79302-18-4 SDS

79302-18-4Relevant academic research and scientific papers

Oxazolo[3',2':1,2]pyrido[3,4-b]indoles and [1,3]-oxazino[3',2':1,2]pyrido[3,4-b]indoles by a simple condensation reaction of 3,4-dihydro-β-carboline with α- and β-hydroxycarboxylic acids

Wanner,Weber

, p. 387 - 390 (1994)

3,4-Dihydro-β-carboline (3) is reacted with trimethylsilyloxyacyl chlorides 2a, 2b, 7 and 11 to give the 1,3-oxazolidin-4-ones 4a/5a and 4b/5b and the 1,3-oxazin-4-ones 8/9 and 12, respectively, representing a new condensation reaction. The enantiomeric p

A Convenient Synthesis of 1,3-Oxazolidin-4-ones and 1,3-Oxazin-4-ones

Wanner, Klaus Th.,Weber, Ulrich

, p. 681 - 683 (2007/10/03)

1,3-Oxazolidin-4-ones and 1,3-oxazin-4-ones were synthesized by formal cyclocondensation of imines with α- or β-hydroxy acids.

Syntheses and Reactions of (Trimethylsiloxy)benzoyl Chlorides

Schwarz, Gerd,Alberts, Heinrich,Kricheldorf, Hans R.

, p. 1257 - 1270 (2007/10/02)

The (trimethylsiloxy)benzoyl chlorides 1-7 are easily to obtain under mild conditions from silylated hydroxybenzoic acids by means of thionyl chloride.Whereas these acid chlorides are stable at room temperature, they undergo condensation polymerisation at temperatures above 100 deg C.Reactions with various nucleophils, such as thioalcohols, phenols, amines, N,O-bis(silylated)amino acids and N-silylated lactams were investigated.With hexamethyldisilazane and thionyl chloride the (trimethylsiloxy)benzonitriles 21, 22 are accessible, and by means of trimethylsilylazide the (trimethylsiloxy)phenyl isocyanates 23-25 were obtained.Conversion with phenyl carbazate and subsequent silylation lead to the 2-(trimethylsiloxy)phenyl-1,3,4-oxadiazol-5-ones 27a-c.

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