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1H-Cyclopropa[b]anthracene is a polycyclic aromatic hydrocarbon (PAH) consisting of a cyclopropane ring fused to an anthracene molecule. It is a colorless solid with a molecular formula of C17H12 and a molecular weight of 216.28 g/mol. 1H-cyclopropa[b]anthracene is characterized by its unique structure, which includes three fused benzene rings and a cyclopropane ring, making it a strained molecule due to the high ring strain in the cyclopropane. 1H-Cyclopropa[b]anthracene is known for its potential mutagenicity and carcinogenicity, as it can interact with DNA and cause mutations. It is also an important compound in the study of organic chemistry, particularly in the synthesis of various complex molecules and the investigation of strained ring systems. Due to its hazardous properties, handling and exposure to 1H-cyclopropa[b]anthracene should be done with caution and proper safety measures.

287-03-6

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287-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287-03-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 287-03:
(5*2)+(4*8)+(3*7)+(2*0)+(1*3)=66
66 % 10 = 6
So 287-03-6 is a valid CAS Registry Number.

287-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopropa[b]anthracene

1.2 Other means of identification

Product number -
Other names 1H-Cycloprop[b]anthracene

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:287-03-6 SDS

287-03-6Downstream Products

287-03-6Relevant academic research and scientific papers

Tricarbonyl-chromium Complexes of Benzannelated Cycloproparenes

Mueller, Paul,Bernardinelli, Gerald,Jacquier, Yvan,Ricca, Alessandra

, p. 1618 - 1626 (1989)

Reaction of 1H-cyclopropanaphthalene (1a) or 1H-cycloporpaanthracene (10a) with tris(acetonitrile)tricarbonylchromium affords cyclobutanaphthalenone and cyclobutaanthracenone 2 and 11, respectively.In contrast, the bis-silylated cycloproparenes 1b and 10b undergo complexation at the terminal benzene ring and lead to the arene-tricarbonylchromium complexes 4b and 12, respectively.Desilylation of 4b to 4a is effected by t-BuOK.

254. Synthesis of Cyclopropanthracenes via Trapping of o-Naphthoquinodimethane

Muller, Paul,Rodriguez, Domingo

, p. 2540 - 2542 (1983)

Cyclopropanthracenes 1, 1a, 1b are prepared in a 3-step synthesis starting from o-di(iodomethyl)benzene.The key step consists of trapping of o-naphthoquinodimethane (9) with 1,2-di- and tetrahalogenocyclopropenes (3, 3a, 4b).

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