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2,5-Cyclohexadiene-1,4-dione, 2-methyl-5-(1-methylethyl)-, 4-oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62094-90-0

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62094-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62094-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,9 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62094-90:
(7*6)+(6*2)+(5*0)+(4*9)+(3*4)+(2*9)+(1*0)=120
120 % 10 = 0
So 62094-90-0 is a valid CAS Registry Number.

62094-90-0SDS

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 2-methyl-4-nitroso-5-propan-2-ylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2-methyl-5-(1-methylethyl)-4-nitroso

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:62094-90-0 SDS

62094-90-0Relevant academic research and scientific papers

The Diels-Alder reactions of para-benzoquinone nitrogen-derivatives: An experimental and theoretical study

Uliana, Marciana P.,Servilha, Bruno M.,Alexopoulos, Olga,De Oliveira, Kleber T.,Tormena, Cláudio F.,Ferreira, Marco A.B.,Brocksom, Timothy J.

, p. 6963 - 6973 (2015/11/09)

An experimental and theoretical study of the comparative reactivity and selectivity of the Diels-Alder reactions of para-benzoquinones and three nitrogen derivatives have been performed. The mono-oximes derivatives do not react under the tested reaction conditions, whereas the tosylated mono-oximes react slowly. However, the mono N-tosyl imines show excellent reactivity, and superior to the parent parabenzoquinones. DFT calculations support these experimental results.

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