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7-methyl-3,4-dihydrobenzo[c]acridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92145-20-5

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92145-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92145-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92145-20:
(7*9)+(6*2)+(5*1)+(4*4)+(3*5)+(2*2)+(1*0)=115
115 % 10 = 5
So 92145-20-5 is a valid CAS Registry Number.

92145-20-5SDS

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 7-methyl-3,4-dihydrobenzo[c]acridine

1.2 Other means of identification

Product number -
Other names -

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:92145-20-5 SDS

92145-20-5Relevant academic research and scientific papers

Synthesis of Potential Metabolites of Dibenzacridine: Dihydro Diols and Phenols

Rosario, Christopher A.,Holder, Gerald M.,Duke, Colin C.

, p. 1064 - 1072 (2007/10/02)

The potential trans dihydro diol metabolites of the carcinogen dibenzacridine (1) were prepared.The dihydro diols trans-1,2-dihydroxydibenzacridine (12) and trans-3,4-dihydro-3,4-dihydroxydibenzacridine (13) were prepared by Prevost reactio

Synthesis of the Non-K-Region Dihydrodiols of 7-Methylbenzacridine

Duke, Colin C.,Murphy, Peter T.,Holder, Gerald M.

, p. 4446 - 4451 (2007/10/02)

The synthesis of the four non-K-region trans-dihydrodiols of 7-methylbenzacridine (2) are described.The trans-8,9- and -10,11-dihydrodiols 13 and 16 were prepared from 7-methyl-8,9,10,11-tetrahydrobenzacridine (3) via the trans-8,9-diacetoxy-7-methyl-8,9,10,11-tetrahydrobenzacridine (10) and its 10,11-isomer (14) by selective benzylic bromination followed by dehydrobromination.The trans-tetrahydro diacetates were obtained through the alkenes 6 and 7 and their epoxide derivatives. trans-1,2- and -3,4-dihydrodiols 22 and 24 were similarly prepared from the trans-1,2- and -3,4-diacetates of 7-methyl-1,2,3,4-tetrahydrobenzacridine (19 and 20).The latter were products of the Prevost reaction on mixed 3,4- and 1,2-dihydro-7-methylbenzacridines (17 and 18).

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