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10-phenyltricyclo<5.3.1.02,6>undeca-3,9-dien-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79562-44-0

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79562-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79562-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,6 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79562-44:
(7*7)+(6*9)+(5*5)+(4*6)+(3*2)+(2*4)+(1*4)=170
170 % 10 = 0
So 79562-44-0 is a valid CAS Registry Number.

79562-44-0Downstream Products

79562-44-0Relevant academic research and scientific papers

Synthesis and Photolysis of Tricyclo2,6>undeca-3,9-dien-8-ones and -4,9-dien-8-ones. Formation of Novel Trishomocubanones

Ogino, Toshio,Awano, Kazuyuki

, p. 2811 - 2818 (2007/10/02)

A series of 10-substituted tricyclo2,6>undeca-3,9-dien-8-ones (6) and the 4,9-dien-8-one isomers (7) were synthesized and photolyzed.Upon irradiation, whereas most of the derivatives underwent photocyclization to give the correspo

Rh(I) CATALYSED CYCLOREVERSION OF TRISHOMOCUBANES

Ogino, Toshio,Awano, Kazuyuki,Ogihara, Tsutomu,Isogai, Koji

, p. 2023 - 2026 (2007/10/02)

Two types of trishomocubanones, pentacyclo2,6.03,10.04,8>undecan-11-ones and pentacyclo2,6.03,10.05,8>undecan-9-ones are catalytically cycloreverted by 2 in different cleavage modes.The mechanism is discussed on the basis of a kinetic study.

INTRAMOLECULAR PHOTOCHEMICAL REACTIONS OF RIGID DIENONES. PREPARATION AND PHOTOLYSIS OF 10-SUBSTITUTED TRICYCLO 2,6> UNDECA-3,9-DIEN-8-ONES AND -4,9-DIEN-8-ONES

Ogino, Toshio,Awano, Kazuyuki

, p. 891 - 894 (2007/10/02)

A series of the title compounds (R=OMe, H, Me, Ph) were prepared and photochemical behaviors of these compounds were examined.Although most of the substrates underwent intramolecular cycloaddition to give novel trishomocubanes upon irradiation, the phenyl derivative of Δ4 isomer gave a product via competing allylic hydrogen abstraction, as well as the cyclization product.

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