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2381-34-2

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2381-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2381-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2381-34:
(6*2)+(5*3)+(4*8)+(3*1)+(2*3)+(1*4)=72
72 % 10 = 2
So 2381-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H14/c1-13-12-15-7-3-5-9-18(15)19-16(13)11-10-14-6-2-4-8-17(14)19/h2-12H,1H3

2381-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methylbenzo[c]phenanthrene

1.2 Other means of identification

Product number -
Other names 1-Methyl-3,4-benzophenanthrene

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:2381-34-2 SDS

2381-34-2Relevant articles and documents

Gold-catalyzed 6-exo-dig cycloisomerization: A versatile approach to functionalized phenanthrenes

Shu, Chao,Li, Long,Chen, Cheng-Bin,Shen, Hong-Cheng,Ye, Long-Wu

supporting information, p. 1525 - 1529 (2014/06/09)

A novel gold-catalyzed 6-exo-dig cycloisomerization of o-propargylbiaryls has been developed that provides ready access to functionalized phenanthrenes in largely good to excellent yields. Notable features of this method are readily available starting materials, mild reaction conditions, and broad substrate scope. Golden cat: A novel gold-catalyzed 6-exo-dig cycloisomerization of o-propargylbiaryls has been developed that provides ready access to functionalized phenanthrenes in largely good to excellent yields. Notable features of this method are readily available starting materials, mild reaction conditions, and broad substrate scope.

Synthesis of a higher fullerene precursor - An "unrolled" C 84 fullerene

Amsharov, Konstantin,Jansen, Martin

scheme or table, p. 2691 - 2693 (2009/09/29)

We report the synthesis of the C84(20)-fullerene related hydrocarbon C84H42, which possesses more than 83% of the C84(20)-fullerene connectivity, and its selective transformation to C84 by flash vacuum pyrolysis (FVP). The Royal Society of Chemistry 2009.

Synthesis of 6,7-benz[c]acephenanthrylene and its photodimerization to a simple molecular tweezer

Magnus, Philip,Morris, Jonathan C.,Lynch, Vince

, p. 506 - 508 (2007/10/03)

A short convenient synthesis of 6,7-benz[c]acephenanthrylene (2) is described. Solutions of C60 (1) in toluene exposed to laboratory lighting readily photodimerize to the cis-cyclobutane 14, with a molecule of toluene intercalated inside the mo

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