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Bicyclo[3.1.0]hexane, 1-phenyl-, also known as 1-phenylbicyclo[3.1.0]hexane, is an organic compound with the molecular formula C12H14. It features a bicyclic structure with a six-membered ring and a three-membered ring fused together, with a phenyl group attached to the first carbon of the six-membered ring. Bicyclo[3.1.0]hexane, 1-phenyl- is a colorless liquid with a density of 1.01 g/cm3 and a boiling point of 240-241°C. It is insoluble in water but soluble in most organic solvents. 1-phenylbicyclo[3.1.0]hexane is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a building block in the development of novel organic compounds and materials.

4669-00-5

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4669-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4669-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4669-00:
(6*4)+(5*6)+(4*6)+(3*9)+(2*0)+(1*0)=105
105 % 10 = 5
So 4669-00-5 is a valid CAS Registry Number.

4669-00-5Downstream Products

4669-00-5Relevant academic research and scientific papers

Synthesis of 1-aryl-2-vinylcycloalkanes by intramolecular carbolithiation

Krief,Remacle,Mercier

, p. 1443 - 1446 (2007/10/03)

Benzyl selenides bearing a side chain possessing in suitable position an allylic ether react with butyllithiums and produce, via the corresponding benzyllithiums, 1-aryl-2-vinylcyclopentanes.

Regioselective syntheses of polycyclic compounds by carbanion-mediated polycyclisation of olefins

Krief,Barbeaux

, p. 417 - 420 (2007/10/02)

This paper reports straightforward syntheses of 1-aryl-bicyclo-[n. 1.0]-alkanes, 1-aryl-bicyclo-[3.3.0]-alkanes and of 1-phenyl-1,4-dimethyl-cyclopentane from unsaturated benzylselenides which involve the organolithiums-mediated cyclisation of olefins and

SYNTHESIS OF FUSED CYCLOPROPANES FROM γ-STANNYL ALCOHOLS

Kadow, John F.,Johnson, Carl R.

, p. 5255 - 5258 (2007/10/02)

Fused cyclopropanes including 3-carene and isosequicarene have been prepared by treatment of γ-stannyl alcohols with thionyl chloride.

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