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10-Methylbenz[c]acridine is a polycyclic aromatic hydrocarbon (PAH) with the chemical formula C21H15N. It is a derivative of benzacridine, featuring a methyl group attached to the 10th carbon atom. 10-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 health concerns, particularly in areas with high levels of pollution or industrial activity. The compound is not approved for use in food, drugs, or cosmetics due to its hazardous properties.

7230-71-9

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7230-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7230-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7230-71:
(6*7)+(5*2)+(4*3)+(3*0)+(2*7)+(1*1)=79
79 % 10 = 9
So 7230-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H13N/c1-12-6-7-14-11-15-9-8-13-4-2-3-5-16(13)18(15)19-17(14)10-12/h2-11H,1H3

7230-71-9SDS

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 9-methylbenz<c>acridine

1.2 Other means of identification

Product number -
Other names 10-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:7230-71-9 SDS

7230-71-9Downstream Products

7230-71-9Relevant academic research and scientific papers

REGIOSELECTIVE THERMAL CYCLIZATION OF 3-SUBSTITUTED ARYLENAMINOIMINE HYDROCHLORIDES, A CONVENIENT METHOD FOR THE SYNTHESIS OF FUCTIONALIZED POLYCYCLIC QUINOLINE DERIVATIVES

Kar, Gandhi K.,Karmakar, Arun C.,Makur, Anindita,Ray, Jayanta K.

, p. 911 - 920 (2007/10/02)

3-Substituted arylenaminoimine hydrochlorides on heating produced exclusively one regioisomer for electron donating groups at 3 position whereas two regioisomers for electron withdrawning/weakly electron donating groups present at the 3 position.

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