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64977-49-7

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64977-49-7 Usage

Type of compound

Polycyclic aromatic hydrocarbon (PAH)

Fluorine substituent position

11th

Methyl group position

5th

Environmental occurrence

Formed during incomplete combustion of organic materials, found in cigarette smoke and grilled foods

Health effects

Potential carcinogen and mutagen

Toxicity

Known for toxic and carcinogenic effects on living organisms

Research focus

Studied for its role in the development of cancer and other health issues related to PAH exposure

Hazardous nature

Requires proper handling and disposal protocols

Check Digit Verification of cas no

The CAS Registry Mumber 64977-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,7 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64977-49:
(7*6)+(6*4)+(5*9)+(4*7)+(3*7)+(2*4)+(1*9)=177
177 % 10 = 7
So 64977-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H13F/c1-12-10-13-6-2-5-9-16(13)19-17(20)11-14-7-3-4-8-15(14)18(12)19/h2-11H,1H3

64977-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoro-11-methylchrysene

1.2 Other means of identification

Product number -
Other names CHRYSENE,11-FLUORO-5-METHYL

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:64977-49-7 SDS

64977-49-7Downstream Products

64977-49-7Relevant articles and documents

Domino synthesis of fluorine-substituted polycyclic aromatic hydrocarbons: 1,1-difluoroallenes as synthetic platforms

Fuchibe, Kohei,Mayumi, Yuka,Zhao, Nan,Watanabe, Shumpei,Yokota, Misaki,Ichikawa, Junji

supporting information, p. 7825 - 7828 (2013/08/23)

Rather crafty: 1,1-Difluoroallenes bearing an aryl group and a cyclopentene moiety undergo indium(III)-catalyzed Friedel-Crafts-type cyclization with subsequent ring expansion and dehydrogenation to afford fluorinated polycyclic aromatic hydrocarbons in high yields. The introduction of an Ar group was effected by in situ halogenation of the intermediary indium species and a subsequent Suzuki-Miyaura reaction. Copyright

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