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1-(tert-butyldimethylsilanyloxy)-2-(tert-butyldimethylsilanyloxymethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82112-31-0

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82112-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82112-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,1 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82112-31:
(7*8)+(6*2)+(5*1)+(4*1)+(3*2)+(2*3)+(1*1)=90
90 % 10 = 0
So 82112-31-0 is a valid CAS Registry Number.

82112-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(tert-butyldimethylsilanyloxy)-2-(tert-butyldimethylsilanyloxymethyl)benzene

1.2 Other means of identification

Product number -
Other names tert-butyl(2-(tert-butyldimethylsilyloxy)benzyloxy)dimethylsilane

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:82112-31-0 SDS

82112-31-0Relevant academic research and scientific papers

PROBE FOR DETECTING CARBAPENEM-RESISTANT BACTERIA AND USE THEREOF

-

Paragraph 0085; 0165-0167, (2021/09/10)

The present disclosure relates to a compound represented by Chemical Formula 1, a probe for detecting antibiotic-resistant bacteria, which includes the compound, a composition containing the compound, a kit including the compound and a method for detectin

Development of carbapenem-based fluorogenic probes for the clinical screening of carbapenemase-producing bacteria

Kim, Juhyeon,Kim, Yihoon,Abdelazem, Ahmed Z.,Kim, Hak Joong,Choo, Hyunah,Kim, Hoon Seok,Kim, Jung Ok,Park, Yeon-Joon,Min, Sun-Joon

, (2019/12/24)

This report describes the synthesis of a library of fluorogenic carbapenemase substrates consisting of carbapenem derivatives, fluorescence dyes, and active cleavable linkers and their evaluation for specifically detecting carbapenemase-producing organism

Highly sulphated cellulose: a versatile, reusable and selective desilylating agent for deprotection of alcoholic TBDMS ethers

Dachavaram, Soma Shekar,Penthala, Narsimha R.,Calahan, Julie L.,Munson, Eric J.,Crooks, Peter A.

supporting information, p. 6057 - 6062 (2018/09/06)

A mild, efficient and rapid protocol was developed for the deprotection of alcoholic TBDMS ethers using a recyclable, eco-friendly highly sulphated cellulose sulphate acid catalyst in methanol. This acid catalyst selectively cleaves alcoholic TBDMS ethers in bis-TBDMS ethers containing both alcoholic and phenolic TBDMS ether moieties.

An Efficient and Highly Chemoselective Method to Desilylate Silyl Ethers

Lee, Adam Shih-Yuan,Yeh, Hsiu-Chih,Yeh, Ming-Kuo,Tsai, Ming-Hung

, p. 919 - 922 (2007/10/03)

An efficient and highly chemoselective desilylating method is described.Trimethylsilyl ethers (0.25 M) in a CH3OH/CCl4 (1:1) solvent mixture are deprotected to their corresponding alcohols with ultrasound in a commercial ultrasonic cleaning bath.Selective deprotection of tert-butyldimethylsilyl ethers of benzyl alcohols and phenols is achieved under ultrasonic conditions.We deprotected also tert-butyldimethylsilyl ethers of primary alcohols, whereas tert-butyldimethylsilyl ethers of secondary and tertiary alcohols are stable under these conditions. - Key words: Sonochemistry; Ultrasound; Cavitation; Desilylation; Chemoselection; Deprotection.

Selective removal of phenolic and alcoholic silyl ethers

Prakash, Chandra,Saleh, Samir,Blair, Lan A.

, p. 7565 - 7568 (2007/10/02)

Potassium carbonate/Kriptofix 222 and pyridinium p-toluenesulfonate or BF3-etherate have been found to remove the tert-butyldimethylsilyl group from phenolic and alcoholic silyl ethers, respectively. This methodology should find wide applicability in complex organic synthesis.

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