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182250-68-6

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  • 3,5 Bis(tert-butyldiphenylsilyloxy)benzoic acidmethylether 20% in toluene

    Cas No: 182250-68-6

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182250-68-6 Usage

General Description

3,5-Bis(tert-butyldiphenylsilyloxy)benzoic acid methyl ester is a chemical compound that is commonly used in organic synthesis and research. It is a derivative of benzoic acid with two tert-butyldiphenylsilyloxy groups attached to the 3 and 5 positions. 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZOIC ACID METHYL ESTER is often utilized as a reagent in the protection and deprotection of hydroxyl groups in organic molecules. It is also used in the synthesis of various biologically active compounds and pharmaceuticals. Additionally, it can serve as a building block for the creation of more complex organic molecules. Overall, 3,5-Bis(tert-butyldiphenylsilyloxy)benzoic acid methyl ester is a versatile and important chemical in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 182250-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,5 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 182250-68:
(8*1)+(7*8)+(6*2)+(5*2)+(4*5)+(3*0)+(2*6)+(1*8)=126
126 % 10 = 6
So 182250-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C40H44O4Si2/c1-39(2,3)45(34-20-12-8-13-21-34,35-22-14-9-15-23-35)43-32-28-31(38(41)42-7)29-33(30-32)44-46(40(4,5)6,36-24-16-10-17-25-36)37-26-18-11-19-27-37/h8-30H,1-7H3

182250-68-6SDS

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 methyl 3,5-bis[[tert-butyl(diphenyl)silyl]oxy]benzoate

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

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More Details:182250-68-6 SDS

182250-68-6Relevant articles and documents

Synthesis of Benzo[ b]furans by Intramolecular C-O Bond Formation Using Iron and Copper Catalysis

Henry, Martyn C.,Sutherland, Andrew

, p. 2766 - 2770 (2020/03/30)

One-pot processes for the synthesis of benzo[b]furans from 1-aryl- or 1-alkylketones using nonprecious transition metal catalysts have been developed. Regioselective iron(III)-catalyzed halogenation of the aryl ring, followed by iron- or copper-catalyzed O-arylation allowed the synthesis of various structural analogues, including the benzo[b]furan-derived natural products corsifuran C, moracin F, and caleprunin B.

Alternative convergent and accelerated double-stage convergent approaches towards functionalized dendritic polyethers

Forier,Dehaen

, p. 9829 - 9846 (2007/10/03)

Alternative convergent synthesis strategies for the preparation of dendritic macromolecules, using either mesylate activation or the Mitsunobu reaction, are described. The synthesis can be further accelerated by using a double stage convergent approach. T

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