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5-Methylbenz[c]acridine is a polycyclic aromatic hydrocarbon (PAH) with the chemical formula C19H15N. It is a derivative of benzacridine, featuring a methyl group attached to the 5th carbon position. 5-Methylbenz[c]acridine is known for its potential mutagenicity and carcinogenicity, as it can interact with DNA and cause mutations. Due to its structural similarity to other PAHs, it is often associated with environmental and occupational health concerns, particularly in settings where incomplete combustion of organic materials occurs, such as in industrial processes or tobacco smoke. The compound's presence in the environment and its impact on human health have been subjects of research, leading to regulations and guidelines aimed at minimizing exposure.

3519-87-7

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3519-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3519-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3519-87:
(6*3)+(5*5)+(4*1)+(3*9)+(2*8)+(1*7)=97
97 % 10 = 7
So 3519-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H13N/c1-12-6-7-13-8-9-15-11-14-4-2-3-5-17(14)19-18(15)16(13)10-12/h2-11H,1H3

3519-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylbenzo[c]acridine

1.2 Other means of identification

Product number -
Other names 5-METHYLBENZ(C)ACRIDINE

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:3519-87-7 SDS

3519-87-7Upstream product

3519-87-7Downstream Products

3519-87-7Relevant academic research and scientific papers

Preparation of aza-polycyclic aromatic compounds via superelectrophilic cyclizations

Li, Ang,Gilbert, Thomas M.,Klumpp, Douglas A.

, p. 3654 - 3657 (2008/09/20)

(Chemical Equation Presented) Alkenyl-substituted N-heterocycles react in superacidic CF3SO3H (triflic acid) to produce dicationic intermediates. These superelectrophiles undergo cyclizations to give varied aza-polycyclic aromatic compounds in generally good yields (27-99%, 16 examples). Theoretical calculations indicate a preference for charge-separated dicationic intermediates.

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