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52899-12-4

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52899-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52899-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,9 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52899-12:
(7*5)+(6*2)+(5*8)+(4*9)+(3*9)+(2*1)+(1*2)=154
154 % 10 = 4
So 52899-12-4 is a valid CAS Registry Number.

52899-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,1-dimethylpropyl)-1,2-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 1,2-dimethyl-4-(1,1-dimethylpropyl)benzene

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:52899-12-4 SDS

52899-12-4Relevant articles and documents

The positional and structural izomerization equilibrium of branched pentylbenzenes

Naumkin,Nesterova,Nesterov,Vodenkova,Golovin

experimental part, p. 141 - 148 (2011/08/05)

The equilibrium of the positional and structural isomerization of branched monopentylbenzenes, pentyltoluenes, and pentyl-o-xylenes was studied. It was found that the 1,2-dimethylpropyl substituted derivatives prevail over the 1,1-dimethylpropyl substituted isomers in the equilibrium mixture of all of the examined groups of compounds. The thermodynamic characteristics of the structural isomerization of pentylbenzenes were calculated from the experimental data.

CHLORINATION OF 4-tert-ALKYL-o-XYLENES

Pozdnyakovich, Yu. V.,Borodovitsyn, V. V.,Shein, S. M.

, p. 138 - 141 (2007/10/02)

The chlorination of 4-tert-butyl-o-xylene and tert-amyl-o-xylene with chlorine and sulfuryl chloride leads to the formation of the products from substitution of the hydrogen atoms at positions 3, 5, and 6 and the tert-alkyl groups at position 4 of the benzene ring.

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