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CAS

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1018955-96-8

6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018955-96-8 Structure

  • Basic information

    1. Product Name: 6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol
    2. Synonyms: 6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol
    3. CAS NO:1018955-96-8
    4. Molecular Formula:
    5. Molecular Weight: 216.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018955-96-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol(1018955-96-8)
    11. EPA Substance Registry System: 6-(4-methoxyphenyl)bicyclo[3.2.0]hept-2-en-6-ol(1018955-96-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1018955-96-8(Hazardous Substances Data)

1018955-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018955-96-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,9,5 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1018955-96:
(9*1)+(8*0)+(7*1)+(6*8)+(5*9)+(4*5)+(3*5)+(2*9)+(1*6)=168
168 % 10 = 8
So 1018955-96-8 is a valid CAS Registry Number.

1018955-96-8Relevant articles and documents

Visible-Light-Mediated Ring-Opening Strategy for the Regiospecific Allylation/Formylation of Cycloalkanols

Wang, Junlei,Huang, Binbin,Shi, Chengcheng,Yang, Chao,Xia, Wujiong

, p. 9696 - 9706 (2018/09/06)

Here we describe a straightforward and efficient approach for regiospecific introduction of an allyl group into cycloalkanol molecules employing a visible-light-mediated ring-opening strategy. A wide range of distally allylated or formylated ketones is fu

An oxidative rearrangement of 6-phenylbicyclo[3.2.0]heptan-6-ol to 1,1′-biphenyl-carbaldehydes: A mechanistic study

Ceylan, Mustafa,Findik, Esra,Secen, Hasan

experimental part, p. 559 - 568 (2009/02/07)

Acid-catalyzed rearrangement of 6-phenylbicyclo[3.2.0]heptan-6-ol gave 1,1′-biphenyl and 1,1′-biphenyl-carbaldehydes in small amounts as well as the expected rearrangement products. A detailed study of the reaction mechanism revealed that the conversion occurs via an oxidative process through the consecutive formation of cycloheptadienes, cycloheptatrienes, and 1,1′-biphenyls. The acid-catalyzed rearrangement of 6-phenylbicyclo[3.2.0] hept-2-en-6-ols gave 1- and 2-phenylcycloheptatrienes directly, from which 1,1′-biphenyl and 1,1′-biphenyl-carbaldehydes were obtained by oxidation.

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