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5,6-Epoxy-5,6-dihydrobenz[a]anthracene is a chemical compound belonging to the class of polycyclic aromatic hydrocarbons (PAHs). It is formed as a result of incomplete combustion of organic materials, such as during the burning of coal, oil, and tobacco. 5,6-EPOXY-5,6-DIHYDROBENZ[A]ANTHRACENE is known to be a potent carcinogen, meaning it can cause cancer in humans and animals. It has been classified as a Group 1 carcinogen by the International Agency for Research on Cancer (IARC). The chemical structure of 5,6-epoxy-5,6-dihydrobenz[a]anthracene consists of a benzene ring fused to an anthracene core, with an epoxy group at the 5,6 positions and a dihydro group at the same positions. Due to its carcinogenic properties, exposure to 5,6-EPOXY-5,6-DIHYDROBENZ[A]ANTHRACENE should be minimized, and it is important to implement safety measures in industries where it may be present.

962-32-3

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962-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 962-32-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 962-32:
(5*9)+(4*6)+(3*2)+(2*3)+(1*2)=83
83 % 10 = 3
So 962-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H12O/c1-2-6-12-10-16-15(9-11(12)5-1)13-7-3-4-8-14(13)17-18(16)19-17/h1-10,17-18H

962-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-benz[a]anthracene-5,6-epoxide

1.2 Other means of identification

Product number -
Other names Benzo-thiazol-dioxid

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:962-32-3 SDS

962-32-3Upstream product

962-32-3Relevant academic research and scientific papers

GENERAL SYNTHETIC ROUTES TO DIARENE OXIDES OF POLYCYCLIC AROMATIC HYDROCARBONS

Agarwal, Shiv K.,Boyd, Derek R.,Jennings, W. Brian,McGuckin, Rosaleen M.,O'Kane, Gerard A.

, p. 123 - 126 (2007/10/02)

Diarene oxides have been synthetized by a single step oxidation of monoarene oxides using dimethyldioxirane, and by a three step cyclization sequence from the appropriate trans-tetrahydrobromoacetate precursors.

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