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1-Phenyltricyclo<4.1.0.0.2,7>heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57293-39-7

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57293-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57293-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,9 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57293-39:
(7*5)+(6*7)+(5*2)+(4*9)+(3*3)+(2*3)+(1*9)=147
147 % 10 = 7
So 57293-39-7 is a valid CAS Registry Number.

57293-39-7Relevant academic research and scientific papers

Preparation of Phenyl-Substituted Derivatives of Tricyclo2,7>heptane and 1,2,3,4-Tetrahydro-1,2,3-methenonaphthalene

Stangl, Roland,Jelinek-Fink, Hans,Christl, Manfred

, p. 479 - 484 (2007/10/02)

The phenyl derivatives 3, 4, and 13 of tricyclo2,7>heptane (1) and 17, 20, and 22 of 1,2,3,4-tetrahydro-1,2,3-methenonaphthalene (2) have been prepared from the dibromocarbene adducts of 1-phenyl-1-cyclohexene, 3-phenyl-1-cyclohexene, 1

ADDITION REACTIONS TO BICYCLOBUTANE DERIVATIVES X. THE REGIOSELECTIVITY AND STEREOSELECTIVITY OF OPENING OF 1-PHENYLTRICYCLO2,7>HEPTANE BY ELECTROPHILIC REAGENTS

Razin, V. V.,Zadonskaya, N. Yu.,Shamurzaev, Kh. T.

, p. 1093 - 1100 (2007/10/02)

The products from the reaction of 1-phenyltricyclo2,7>heptane with sulfuric acid, mercury(II) acetate, and N-bromosuccinimide in an aqueous and/or methanol medium were studied.The addition of methanol catalyzed by sulfuric acid takes pl

Nickel(0)-Catalyzed Cross Coupling Reactions of (Tricyclo2,7>hept-1-yl)magnesium Bromide and Related Grignard Reagents with Aryl, Vinyl, and Alkynyl Halides

Kottirsch, Georg,Szeimies, Guenter

, p. 1495 - 1505 (2007/10/02)

(Tricyclo2,7>hept-1-yl)magnesium bromide (1c) and similar Grignard reagents like 2c, 3a-d, and 4 were cross-coupled with a series of aryl, vinyl, and alkynyl chlorides or bromides in the presence of approximately 1percent of nickel dichloride (NidppeCl2) leading to bridgehead-substituted aryl-, vinyl-, and alkynylbicyclobutanes in varying yields.

REACTIONS OF CARBENES WITH COMPOUNDS OF THE BICYCLOBUTANE SERIES. II. REACTION OF DICHLOROCARBENE WITH TRICYCLO2,7>HEPTANES

Koptelov, Yu. B.,Kostikov, R. R.,Molchanov, A. P.

, p. 2181 - 2185 (2007/10/02)

Dichlorocarbene generated under the conditions of phase-transfer catalysis reacts with unsubstituted 1-methyl- and 1-phenyltricyclo2,7>heptanes with the formation of 2-substituted 3-(2,2-dichlorovinyl)-1-cyclohexenes and 1-substituted 7

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