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CAS

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64036-31-3

2-Phenanthrenol, 1,2,3,4-tetrahydro-, benzoate, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64036-31-3 Structure

  • Basic information

    1. Product Name: 2-Phenanthrenol, 1,2,3,4-tetrahydro-, benzoate, (2S)-
    2. Synonyms:
    3. CAS NO:64036-31-3
    4. Molecular Formula: C21H18O2
    5. Molecular Weight: 302.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64036-31-3.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: 2-Phenanthrenol, 1,2,3,4-tetrahydro-, benzoate, (2S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Phenanthrenol, 1,2,3,4-tetrahydro-, benzoate, (2S)-(64036-31-3)
    11. EPA Substance Registry System: 2-Phenanthrenol, 1,2,3,4-tetrahydro-, benzoate, (2S)-(64036-31-3)

  • 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: 64036-31-3(Hazardous Substances Data)

64036-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64036-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64036-31:
(7*6)+(6*4)+(5*0)+(4*3)+(3*6)+(2*3)+(1*1)=103
103 % 10 = 3
So 64036-31-3 is a valid CAS Registry Number.

64036-31-3Downstream Products

64036-31-3Relevant articles and documents

Enantioselectivity in the reduction of tricyclic hydroaromatic ketones by baker's yeast

Fontana, Gabriele,Manitto, Paolo,Speranza, Giovanna,Zanzola, Simona

, p. 1381 - 1387 (1998)

Three benzo-2-tetralones were hydrogenated to the corresponding alcohols by non-fermenting baker's yeast. Satisfactory yields but modest enantioselectivities were observed. The prevalent enantioform of the benzo- 2-tetralol was found to be in agreement with the predictive abstract model previously proposed for the enzymatic hydrogenation of aromatic ring substituted 2-tetralones.

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