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2091-91-0

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2091-91-0 Usage

Chemical structure

1,2,3,4,5,6-hexahydrochrysene is a polycyclic aromatic hydrocarbon (PAH) that consists of six fused benzene rings.

Toxicity

It is a highly toxic and potentially carcinogenic chemical.

Classification

It is classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC).

Sources

1,2,3,4,5,6-hexahydrochrysene is primarily found in coal tar, and it can also be formed as a byproduct of the incomplete combustion of organic materials, such as fossil fuels and tobacco.

Health effects

Exposure to 1,2,3,4,5,6-hexahydrochrysene has been linked to various adverse health effects, including lung damage, skin irritation, and genetic mutations.

Risk reduction

Due to its harmful nature, efforts are being made to reduce occupational and environmental exposures to this hazardous chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 2091-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2091-91:
(6*2)+(5*0)+(4*9)+(3*1)+(2*9)+(1*1)=70
70 % 10 = 0
So 2091-91-0 is a valid CAS Registry Number.

2091-91-0SDS

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 1,2,3,4,5,6-HEXAHYDROCHRYSENE

1.2 Other means of identification

Product number -
Other names 1,2,3,4,5,6-hexahydrochryzene

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:2091-91-0 SDS

2091-91-0Relevant articles and documents

Synthesis of Nitropolycyclic Aromatic Hydrocarbons with the Substituent at the Longest Axis

Miller, Dwight W.,Herreno-Saenz, Diogenes,Huang, Kurt H.,Heinze, Thomas M.,Fu, Peter P.

, p. 3746 - 3748 (2007/10/02)

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SYNTHESIS OF CHRYSENES AND OTHER a-FUSED PHENANTHRENES BY A PALLADIUM(O) COUPLING-ELECTROCYCLIC RING CLOSURE SEQUENCE

Gilchrist, Thomas L.,Summersell, Richard J.

, p. 2595 - 2602 (2007/10/02)

2-Bromo-1-vinyl-3,4-dihydronaphthalene (1a) has been coupled with several vinyl-, aryl-, and heteroaryl-zinc halides in the presence of tetrakis(triphenylphosphine)palladium(O) to give the corresponding 2-vinyl-, 2-aryl-, and 2-heteroaryl-naphthalenes in

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