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(2S)-2-hydroxy-8-methoxy-1,2,3,4-tetrahydronaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 460740-16-3 Structure
  • Basic information

    1. Product Name: (2S)-2-hydroxy-8-methoxy-1,2,3,4-tetrahydronaphthalene
    2. Synonyms:
    3. CAS NO:460740-16-3
    4. Molecular Formula:
    5. Molecular Weight: 178.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 460740-16-3.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: (2S)-2-hydroxy-8-methoxy-1,2,3,4-tetrahydronaphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-2-hydroxy-8-methoxy-1,2,3,4-tetrahydronaphthalene(460740-16-3)
    11. EPA Substance Registry System: (2S)-2-hydroxy-8-methoxy-1,2,3,4-tetrahydronaphthalene(460740-16-3)
  • 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: 460740-16-3(Hazardous Substances Data)

460740-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 460740-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,7,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 460740-16:
(8*4)+(7*6)+(6*0)+(5*7)+(4*4)+(3*0)+(2*1)+(1*6)=133
133 % 10 = 3
So 460740-16-3 is a valid CAS Registry Number.

460740-16-3Relevant articles and documents

A chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralins

Orsini, Fulvia,Sello, Guido,Travaini, Elena,Di Gennaro, Patrizia

, p. 253 - 259 (2002)

(2R)-2-Amino-8-methoxy-1,2,3,4-tetrahydronaphthalene, a useful precursor of the 5-hydroxytryptamine receptor agonist 8-OH-DPAT ((2R)-2-(dipropylamino)-8-hydroxytetrahydronaphthalene), has been synthesized from 1-methoxynaphthalene through a chemoenzymatic protocol. The same protocol has been subsequently applied to the synthesis of other (2R)-2-amino-1,2,3,4-tetrahydronaphthalenes.

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