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12-methylbenzo[e]acephenanthrylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95741-47-2

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95741-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95741-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,4 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95741-47:
(7*9)+(6*5)+(5*7)+(4*4)+(3*1)+(2*4)+(1*7)=162
162 % 10 = 2
So 95741-47-2 is a valid CAS Registry Number.

95741-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylbenzo[e]acephenanthrylene

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:95741-47-2 SDS

95741-47-2Downstream Products

95741-47-2Relevant academic research and scientific papers

Attempted synthesis of Fjord-region containing polycyclic fluoranthenes reveals a steric-driven double Wagner-Meerwein rearrangement

Cho, Bongsup P.,Zhou, Li

, p. 1535 - 1538 (2007/10/03)

A double Wagner-Meerwein rearrangement takes place commonly in the synthesis of sterically hindered polycyclic fluoranthenes via cyclodehydration reactions and the extent of intramolecular steric crowding within the initially formed tertiary cationic intermediate controls the equilibrium between the expected and the rearranged product.

Synthesis of Methylated Benzofluoranthenes and Benzofluoranthenes

Amin, Shantu,Huie, Keith,Hussain, Nalband,Balanikas, George,Hecht, Stephen S.

, p. 1948 - 1954 (2007/10/02)

A series of monomethyl and dimethyl derivatives of benzofluoranthene (BbF) and benzofluoranthene (BkF) were synthesized in order to investigate the enviromental occurence and structural requirements for carcinogenicity of methylated nonalternant polycyclic aromatic hydrocarbons. 9-Methyl-BbF (5), 12-methyl-BbF (6), and 1-methyl-BbF (7) were prepared from the appropriate oxotetrahydro-BbF's (17-19). 8-Methyl-BbF (8) was synthesized from 1-methyl-3-oxo-1,2,3,10b-tetrahydrofluoranthene (20) in 11 steps. 3-Methyl-BbF (9) and 1,3-dimethyl-BbF (10) were prepared from 3-methyl-1-oxo-1,2,3,3a-tetrahydrobenzofluoranthene (31), which was synthesized from methyl 11H-benzofluorene-11-carboxylate (28). 7-Methyl-BbF (11) was obtained by condensation of 1-methylfluorene (33) with o-bromobenzaldehyde, followed by treatment with KOH and quinoline. 5,6-Dimethyl-BbF (12) was synthesized by reaction of 2,3-dimethylbutadiene with acephenanthrylene (38) followed by aromatization. 8-Methyl-BkF (13) was synthesized from 8-oxo-8,9,10,11-tetrahydro-BkF. 9-Methyl-BkF (14) was prepared by Friedel-Crafts reaction of 2-methylsuccinic anhydride with fluoranthene, followed by Wolff-Kishner reduction, cyclization, LiAlH4 reduction, dehydration, and aromatization. 2-Methyl-BkF (16) was synthesized by an analogous sequence, beginning with 2-methylfluoranthene and succinic anhydride. 7,12-Dimethyl-BkF (15) was prepared by a two-step reduction of 7,12-dicyano-BkF (51).

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