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Cyclohexanone, O-[(1,1-dimethylethyl)dimethylsilyl]oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112933-52-5

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112933-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112933-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,3 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112933-52:
(8*1)+(7*1)+(6*2)+(5*9)+(4*3)+(3*3)+(2*5)+(1*2)=105
105 % 10 = 5
So 112933-52-5 is a valid CAS Registry Number.

112933-52-5SDS

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 Cyclohexanone O-(tert-butyldimethylsilyl)oxime

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:112933-52-5 SDS

112933-52-5Downstream Products

112933-52-5Relevant academic research and scientific papers

A convenient method for the synthesis of O-tert-butyldimethylsilyl oximes

Ortiz,Cordero,Pinto,Alverio

, p. 409 - 415 (2007/10/02)

Aromatic, aliphatic, cyclic and acyclic O-tert-butyldimethylsilyl oximes were prepared in 77 to 85% yield by the reaction of the corresponding aldoximes and ketoximes with tert-butyldimethylchlorosilane (TBSCI) using imidazole/DMF system.

A New Synthesis of Oxime Derivatives from Carbonyl Compounds and N,O-Bis(trimethylsilyl)hydroxylamine

Hoffman, Robert V.,Buntain, Gregory A.

, p. 831 - 833 (2007/10/02)

Reaction of a series of aldehydes and ketones with the potassium salt of N,O-bis(trimethylsilyl)hydroxylamine (2) gave high yields of the corresponding oximate anion 5.This anion, formed in a Peterson-type reaction, could be protonated to the oxime 7 or trapped in situ with a variety of electrophiles to give O-substituted oxime derivatives.

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