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3074-00-8

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3074-00-8 Usage

Uses

6H-Benzo[cd]pyren-6-one is a polycyclic aromatic hydrocarbon ketone that has fluorescent properties and is a common air contaminant. It is also a potentially carcinogenic and polar constituent of carbon black.

Safety Profile

Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors.

Check Digit Verification of cas no

The CAS Registry Mumber 3074-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3074-00:
(6*3)+(5*0)+(4*7)+(3*4)+(2*0)+(1*0)=58
58 % 10 = 8
So 3074-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H10O/c20-19-14-5-1-3-11-7-9-13-10-8-12-4-2-6-15(19)17(12)18(13)16(11)14/h1-10H

3074-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6H-benzo[cd]pyren-6-one

1.2 Other means of identification

Product number -
Other names 6H-Benzo[cd]pyrene-6-one

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:3074-00-8 SDS

3074-00-8Relevant articles and documents

The synthesis and STM/AFM imaging of 'Olympicene' benzo[cd]pyrenes

Mistry, Anish,Moreton, Ben,Schuler, Bruno,Mohn, Fabian,Meyer, Gerhard,Gross, Leo,Williams, Antony,Scott, Peter,Costantini, Giovanni,Fox, David J.

supporting information, p. 2011 - 2018 (2015/01/30)

H-Benzo[cd ]pyrene ('Olympicene') is a polyaromatic hydrocarbon and non-Kekul fragment of graphene. A new synthetic method has been developed for the formation of 6H-benzo[cd]pyrene and related ketones including the first time isolation of the unstable alcohol 6H-benzo[cd]pyren-6-ol. Molecular imaging of the reaction products with scanning tunnelling microscopy (STM) and non-contact atomic force microscopy (NC-AFM) characterised the 6H-benzo[cd]pyrene as well as the previously intangible and significantly less stable 5 H-benzo[cd ]pyrene, the fully conjugated benzo[cd]pyrenyl radical and the ketones as oxidation products.

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