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1,3,5-Cycloheptatriene, 3-phenyl- is an organic compound with the molecular formula C13H14. It is a derivative of cycloheptatriene, a seven-membered ring with three double bonds, and features a phenyl group (C6H5) attached to the third carbon atom. 1,3,5-Cycloheptatriene, 3-phenyl- is known for its aromatic properties and can undergo various chemical reactions due to the presence of the phenyl group. It is used in the synthesis of other organic compounds and has potential applications in the pharmaceutical and chemical industries. The compound is characterized by its unique structure, which combines the properties of both cycloheptatriene and benzene, making it an interesting subject for study in organic chemistry.

1541-13-5

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1541-13-5 Usage

Structure

Cyclic hydrocarbon with a seven-membered ring and a phenyl group attached at the 3-position

Physical state

Colorless liquid at room temperature

Usage

Building block in organic synthesis

Applications

Potential use in the development of new pharmaceuticals and materials

Aromatic properties

Known for its aromatic properties and used as a starting material for the synthesis of various aromatic compounds

Safety precautions

Should be handled with care and following proper safety procedures due to its reactivity and potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 1541-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1541-13:
(6*1)+(5*5)+(4*4)+(3*1)+(2*1)+(1*3)=55
55 % 10 = 5
So 1541-13-5 is a valid CAS Registry Number.

1541-13-5Relevant academic research and scientific papers

Direct Proton-Transfer Reaction via a Transient Hydrogen Bond Bridged Allyl Anion System on the Models of Cycloheptatrienes and Propene

Takahashi, Kazuko,Suzuki, Tsuyoshi,Toda, Hideo,Takase, Kahei,Koseki, Shiro,Nakajima, Takeshi

, p. 2666 - 2673 (2007/10/02)

The base-catalyzed intramolecular proton transfer in cycloheptatriene derivatives and propene has been investigated both theoretically and experimentally.A direct 1,3-intramolecular proton shift was observed in cycloheptatriene derivatives, the shift proc

Chemistry of some Bridged Bicyclobut-1(3)-ene Derivatives

Schlueter, Arnulf-Dieter,Harnisch, Hanna,Harnisch, Joachim,Szeimies-Seebach, Ursula,Szeimies, Guenter

, p. 3513 - 3528 (2007/10/02)

Tricyclo2,6>hex-1(6)-ene (3), benzotricyclo2,7>hepta-1(7),3-diene (4) and tetracyclo2,4.03,5>hept-3-ene (5) were generated as short-lived intermediates by methods, which had proved suc

Base-catalysed isomerization of 7-phenyl-1,3,5-cycloheptatriene

Zwaard, A. W.,Prins, M. D.,Kloosterziel, H.

, p. 188 - 192 (2007/10/02)

Under the influence of basic alcohol, 7-phenyl-1,3,5-cycloheptatriene (7c) forms its 1-, 2- and 3-isomers (viz. 1c, 2c and 3c) in parallel reactions, contrary to suggestions made in the literature.The activation parameters for these reactions are given.The difference in behaviour (in isomerization and exchange reactions under basic conditions) between 7-(methoxycarbonyl)-1,3,5-cycloheptatriene (7b) and 7-phenyl-1,3,5-cyclopentatriene (7c) is explained by the weaker electron-attracting properties of the phenyl ring as compared to the methoxycarbonyl substituent.

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