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1,2'-Binaphthalene, 1,1',2,2',3,3',4,4'-octahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91598-34-4

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91598-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91598-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91598-34:
(7*9)+(6*1)+(5*5)+(4*9)+(3*8)+(2*3)+(1*4)=164
164 % 10 = 4
So 91598-34-4 is a valid CAS Registry Number.

91598-34-4SDS

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 1,2'-Binaphthalene, 1,1',2,2',3,3',4,4'-octahydro-

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:91598-34-4 SDS

91598-34-4Upstream product

91598-34-4Downstream Products

91598-34-4Relevant academic research and scientific papers

Product, Radical Intermediates, and Hydrogen Atom Production in the Thermal Decomposition of 1,2-Dihydronaphthalene

Franz, James A.,Camaioni, Donald M.,Beishline, Robert R.,Dalling, Don K.

, p. 3563 - 3570 (2007/10/02)

The thermal decomposition of 1,2-dihydronaphthalene (DHN) at 300 deg C produces tetralin, naphthalene, hydrogen and five C20 hydrocarbon products (1-5).The isolation of compounds 1-5 from the thermal decomposition of 1,2-dihydronaphthalene-4-d revealed compounds 1 and 2 to be formed by the addition of 2-hydronaphtyl (2HN) to DHN followed by intramolecular cyclization and hydrogen abstraction.Compound 3 was formed by addition of 1-tetralyl radical to DHN followed by hydrogen abstraction, and compounds 4 and 5 were formed by a sequence involving initial addition of 2-tetralyl radical to dihydronaphthalene.The thermal decomposition of DHN at 400-450 deg C leads to the formation of a hydrogen atom which participates in subsequent hydrocracking reactions of available substituted aromatic structures.

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