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2717-39-7

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2717-39-7 Usage

Uses

1,4,5,8-Tetramethylnaphthalene is a compound found in coal tar.

Check Digit Verification of cas no

The CAS Registry Mumber 2717-39-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2717-39:
(6*2)+(5*7)+(4*1)+(3*7)+(2*3)+(1*9)=87
87 % 10 = 7
So 2717-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16/c1-9-5-6-11(3)14-12(4)8-7-10(2)13(9)14/h5-8H,1-4H3

2717-39-7SDS

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 1,4,5,8-Tetramethylnaphthalene

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:2717-39-7 SDS

2717-39-7Relevant articles and documents

Reaction routes in catalytic reforming of poly(3-hydroxybutyrate) into renewable hydrocarbon oil

Kang, Shimin,Yu, Jian

, p. 30005 - 30013 (2015/05/13)

Poly(3-hydroxybutyrate) or PHB is an energy storage material of microbial organisms and can be reformed into hydrocarbon oils rich with aromatic compounds. This work investigated the main reaction routes from PHB to the key intermediates and final hydrocarbons. The main sequential reactions under catalysis of phosphoric acid at moderate temperatures (200-230 °C) consist of: (1) decomposition of PHB into crotonic acid, a major monomeric intermediate, (2) deoxygenation of crotonic acid, and (3) combination of the deoxygenated molecules. The oxygen in PHB is removed as CO2 and H2O in stage (2), involving decarboxylation and ketonization of crotonic acid. The main aromatic compounds are formed in stage (3) from propylene and 2,3-dimethyl-2-cyclopenten-1-one as two key intermediates, the former from decarboxylation and the latter from ketonization of crotonic acid. The reaction routes reveal that the formation of aromatics is affected to a great extent by the concentrations of phosphoric acid and water in the reaction, which can be used to control the composition of hydrocarbon oil.

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