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1,2,3,6,7,8-hexahydro-as-indacene is a polycyclic aromatic hydrocarbon (PAH) with a unique molecular structure consisting of six fused benzene rings and six hydrogen atoms. It is a derivative of as-indacene, which is a tricyclic compound with a central benzene ring and two attached five-membered rings. The hexahydro prefix indicates that there are six hydrogen atoms added to the molecule, which are typically located at the positions where the benzene rings are fused together. 1,2,3,6,7,8-hexahydro-as-indacene is of interest in organic chemistry and materials science due to its potential applications in the development of new materials and its structural similarity to other PAHs, which are known for their electronic and optical properties. However, it is important to note that the specific properties, reactivity, and applications of 1,2,3,6,7,8-hexahydro-as-indacene would need to be further investigated through experimental studies.

1076-17-1

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1076-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1076-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1076-17:
(6*1)+(5*0)+(4*7)+(3*6)+(2*1)+(1*7)=61
61 % 10 = 1
So 1076-17-1 is a valid CAS Registry Number.

1076-17-1SDS

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 1,2,3,6,7,8-hexahydro-as-indacene

1.2 Other means of identification

Product number -
Other names Benzo<1,2:3,4>dicyclopenten

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:1076-17-1 SDS

1076-17-1Downstream Products

1076-17-1Relevant academic research and scientific papers

Intramolecular thermal cyclotrimerization of an acyclic triyne: An uncatalyzed process

Kociolek, Martin G.,Johnson, Richard P.

, p. 4141 - 4144 (1999)

Flash vapor pyrolysis of 1,6,11-dodecatriyne at 500 to 600 °C and 0.01 torr affords 1,2,3,6,7,8-Hexahydro-[as]-indacene and dehydro derivatives. An uncatalyzed and highly exothermic two-step cycloaromatization mechanism is suggested. This proceeds through initial formation of a 1,4-diradical.

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