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2,6-Bis(trimethylsilyloxy)benzoic acid trimethylsilyl ester is a complex organic compound with the chemical formula C15H26O4Si3. It is a derivative of benzoic acid, featuring two trimethylsilyloxy groups at the 2 and 6 positions on the benzene ring, and a trimethylsilyl ester group at the carboxylic acid position. 2,6-Bis(trimethylsilyloxy)benzoic acid trimethylsilyl ester is known for its stability and is often used in organic synthesis, particularly in the protection of carboxylic acids and in the formation of esters. Its unique structure allows it to participate in various chemical reactions, making it a valuable intermediate in the synthesis of more complex molecules.

3782-85-2

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3782-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3782-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3782-85:
(6*3)+(5*7)+(4*8)+(3*2)+(2*8)+(1*5)=112
112 % 10 = 2
So 3782-85-2 is a valid CAS Registry Number.

3782-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylsilyl 2,6-bis((trimethylsilyl)oxy)benzoate

1.2 Other means of identification

Product number -
Other names trimethylsilyl 2,6-bis[(trimethylsilyl)oxy]benzoate

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

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More Details:3782-85-2 SDS

3782-85-2Downstream Products

3782-85-2Relevant academic research and scientific papers

Synthesis of trimethylsilyl carboxylates by HMDS under solvent-free conditions

Jereb, Marjan,Lakner, Janja

, p. 5713 - 5723 (2016/08/23)

A broad set of structurally different carboxylic acids were transformed into their trimethylsilyl esters with HMDS in a practically completely solvent-free process, while a catalytic amount of iodine was required in some cases. The process has several advantages over the known methods: untreated reactants, air atmosphere, mild and neutral conditions, no evolution of hydrogen halide, no need of an additional base, low amount of waste, completely without chromatography, low consumption of energy, and operational simplicity.

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