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10-hydroxy-1,4,5,8-tetrahydro-4a,8a-ethanonaphthalen-9-one is a hydroxy derivative of tetrahydronaphthalene with a ketone functional group. It is an organic compound that appears as a white to off-white crystalline powder and is soluble in organic solvents such as ethanol, methanol, and chloroform.

7195-63-3

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7195-63-3 Usage

Uses

Used in Pharmaceutical Industry:
10-hydroxy-1,4,5,8-tetrahydro-4a,8a-ethanonaphthalen-9-one is used as a building block in the synthesis of complex organic compounds for pharmaceutical applications. Its chemical structure and properties make it suitable for the development of new drugs and therapeutic agents.
Used in Perfumery Industry:
10-hydroxy-1,4,5,8-tetrahydro-4a,8a-ethanonaphthalen-9-one is used as a precursor for the production of various fragrances and perfumes. Its unique chemical structure contributes to the creation of distinct scents and aromas.
Used in Agrochemical Industry:
10-hydroxy-1,4,5,8-tetrahydro-4a,8a-ethanonaphthalen-9-one is used as a precursor for the production of agrochemicals, such as pesticides and herbicides. Its chemical properties make it a valuable component in the development of effective and environmentally friendly agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 7195-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7195-63:
(6*7)+(5*1)+(4*9)+(3*5)+(2*6)+(1*3)=113
113 % 10 = 3
So 7195-63-3 is a valid CAS Registry Number.

7195-63-3Relevant academic research and scientific papers

Synthetic studies on the 1,6-methano[10]annulene skeleton: A new route that provides derivatives substituted at the bridge and on the annulene ring

Barrett, David G.,Liang, Gui-Bai,McQuade, D. Tyler,Desper, John M.,Schladetzky, Kurt D.,Gellman, Samuel H.

, p. 10525 - 10532 (2007/10/02)

A new synthetic route to the 1,6-methano[10]annulene skeleton has been developed. The key step in this route is the semi-benzylic Favorskii rearrangement of a [4.4.2]propellane to a [4.4.1]propellane. The methodology discussed here provides access to 1,6-

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