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1432-30-0

Naphthalene, 2-(2-[1,1'-biphenyl]-4-ylethenyl)-, also known as 2-(2-[1,1'-biphenyl]-4-ylethenyl)naphthalene, is an organic compound with the molecular formula C20H14. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and features a biphenyl-4-ylethenyl group attached to the 2-position of the naphthalene ring. Naphthalene, 2-(2-[1,1'-biphenyl]-4-ylethenyl)- is characterized by its planar structure and conjugated π-electron system, which contributes to its electronic properties and potential applications in various fields, such as organic electronics and materials science. Due to its complex structure and potential reactivity, it is important to handle Naphthalene, 2-(2-[1,1'-biphenyl]-4-ylethenyl)- with care, following appropriate safety guidelines.

1432-30-0

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1432-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1432-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1432-30:
(6*1)+(5*4)+(4*3)+(3*2)+(2*3)+(1*0)=50
50 % 10 = 0
So 1432-30-0 is a valid CAS Registry Number.

1432-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-phenylphenyl)ethenyl]naphthalene

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:1432-30-0 SDS

1432-30-0Relevant articles and documents

Nickel-catalyzed synthesis of (E)-olefins from benzylic alcohol derivatives and arylacetonitriles via C-O activation

Xiao, Jing,Yang, Jia,Chen, Tieqiao,Han, Li-Biao

, p. 2157 - 2160 (2016/02/05)

An efficient Ni-catalyzed synthesis of (E)-olefins using the readily available benzylic alcohol derivatives and arylacetonitriles is described. This transformation should proceed via a tandem process involving nickel-catalyzed cross coupling via C-O activation and subsequent stereoselective E2 elimination.

Highly efficient fluorine-promoted intramolecular condensation of benzo[c]phenanthrene: A new prospective on direct fullerene synthesis

Amsharov, Konstantin Yu.,Kabdulov, Mikhail A.,Jansen, Martin

experimental part, p. 6328 - 6335 (2011/03/19)

Various functional groups have been tested as alternative promoters of the intramolecular condensation of benzo-[c]phenanthrene under flash vacuum pyrolysis conditions. Methyl and fluorine functionalization were found to be promising approaches. Unexpectedly high selectivity was observed in the cyclization of fluorinated benzo[c]phenanthrenes. The mechanism for the condensation reaction and the advantages of fluorine as a promoter for the rational synthesis of fullerenes are discussed. Wiley-VCH Verlag GmbH & Co. KGaA.

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