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211-91-6

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211-91-6 Usage

Uses

Benz[l]aceanthrylene is a mutagenic agent.

Safety Profile

Mutation data reported. Whenheated to decomposition it emits acrid smoke and fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 211-91-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 211-91:
(5*2)+(4*1)+(3*1)+(2*9)+(1*1)=36
36 % 10 = 6
So 211-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H12/c1-2-7-17-13(4-1)8-9-16-12-15-6-3-5-14-10-11-18(19(14)15)20(16)17/h1-12H

211-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Benz(l)aceanthrylene

1.2 Other means of identification

Product number -
Other names Benzo<aceanthrylen

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:211-91-6 SDS

211-91-6Downstream Products

211-91-6Relevant articles and documents

Synthesis of a Series of Novel Polycyclic Aromatic Systems: Isomers of Benzanthracene Containing a Cyclopenta-Fused Ring

Sangaiah, R.,Gold, A.,Toney, G. E.

, p. 1632 - 1638 (2007/10/02)

The four possible isomers of benzanthracene containing a cyclopenta-fused ring have been synthesized and characterized.These systems are of interest for structure-activity studies in bioactivation because of their predicted high level of activity.Formation of fused five-membered rings by intramolecular cyclodehydration, often difficult to accomplish, was found to be smoothly effected in anhydrous HF, provided the reactivity index (Nt) for the appropriate electrophilic addition was favorable.The dihydro polycyclic aromatic alcohols obtained from reduction of the c orresponding keto cyclodehydration products were best dehydrated to the desired PAH by activity grade I neutral alumina in refluxing benzene.This dehydration proceeds in high yield without the formation of isomeric or polymeric side products that occurred even under such mild acid catalysis as p-toluenesulfonic acid.

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