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CAS

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125101-72-6

3,3-dibenzyloxy-4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125101-72-6 Structure

  • Basic information

    1. Product Name: 3,3-dibenzyloxy-4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone
    2. Synonyms:
    3. CAS NO:125101-72-6
    4. Molecular Formula:
    5. Molecular Weight: 362.469
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125101-72-6.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: 3,3-dibenzyloxy-4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-dibenzyloxy-4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone(125101-72-6)
    11. EPA Substance Registry System: 3,3-dibenzyloxy-4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone(125101-72-6)

  • 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: 125101-72-6(Hazardous Substances Data)

125101-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125101-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,0 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125101-72:
(8*1)+(7*2)+(6*5)+(5*1)+(4*0)+(3*1)+(2*7)+(1*2)=76
76 % 10 = 6
So 125101-72-6 is a valid CAS Registry Number.

125101-72-6Relevant articles and documents

A new entry to the synthesis of 1,2-benzenediol congeners

Ozaki,Oshio,Ohsuga,Kaburagi,Sung,Kim

, p. 1132 - 1136 (2007/10/02)

1,2-Benzenediols were synthesized via 1,1-bis(ethylthio)-3-cyclohexen-2-one derivatives, which were prepared by condensation of 1,1-bis(ethylthio)-2-propanone with Mannich bases. Regioselective preparation of their monoethers was also achieved.

A NEW ENTRY TO 1,2-BENZENEDIOL CONGENERS

Ozaki, Yutaka,Oshio, Ikumi,Kim, Sang-Won

, p. 1434 - 1436 (2007/10/02)

1,2-Benzenediols and their monoethers were efficiently prepared from α,α-bis(ethylthio)cyclohexenones which were constructed by the C3+C3 annulation of 1,1-bis(ethylthio)propan-2-one and the Mannich bases. KEYWORDS 1,2-benzenediol; aromatic synthesis; annulation; aromatic compound; acetal

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