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58901-83-0

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58901-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58901-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58901-83:
(7*5)+(6*8)+(5*9)+(4*0)+(3*1)+(2*8)+(1*3)=150
150 % 10 = 0
So 58901-83-0 is a valid CAS Registry Number.

58901-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-3-[4-(2-methylpropyl)phenyl]oxirane-2-carbonitrile

1.2 Other means of identification

Product number -
Other names Oxiranecarbonitrile,3-methyl-3-[4-(2-methylpropyl)phenyl]

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:58901-83-0 SDS

58901-83-0Relevant articles and documents

REACTION OF 4-SUBSTITUTED BENZALDEHYDES AND ACETOPHENONES WITH CHLOROACETONITRILE

Svoboda, Jiri,Kocfeldova, Zuzana,Palecek, Jaroslav

, p. 822 - 832 (2007/10/02)

Under conditions of phase-transfer catalysis or in homogeneous solution of potassium tert-butoxide the title compounds give stereoisomeric mixtures of substituted 2,3-epoxy nitriles III and IV.Alkaline hydrolysis of epoxy nitriles IV afforded the corresponding 2-arylpropanals in low yields.On treatment with methanol and potassium carbonate, epoxy nitriles III and IV were converted into epoxy esters in good yields.

Process for preparing glycidonitriles

-

, (2008/06/13)

Process for preparing glycidonitriles in which a ketone or aldehyde is reacted with chloroacetonitrile under substantially anhydrous conditions using inorganic alkali metal bases in a solvent medium containing at least about 3 percent liquid volume of a dipolar, aprotic liquid such as dimethylformamide, any balance of solvent being a nonpolar organic liquid.

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