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CAS

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94152-63-3

(5alpha)-3-methoxy-4,5-epoxymorphinan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94152-63-3 Structure

  • Basic information

    1. Product Name: (5alpha)-3-methoxy-4,5-epoxymorphinan
    2. Synonyms:
    3. CAS NO:94152-63-3
    4. Molecular Formula: C17H21NO2
    5. Molecular Weight: 271.3541
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94152-63-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 427.4°C at 760 mmHg
    3. Flash Point: 174.1°C
    4. Appearance: N/A
    5. Density: 1.25g/cm3
    6. Vapor Pressure: 1.64E-07mmHg at 25°C
    7. Refractive Index: 1.626
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (5alpha)-3-methoxy-4,5-epoxymorphinan(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5alpha)-3-methoxy-4,5-epoxymorphinan(94152-63-3)
    12. EPA Substance Registry System: (5alpha)-3-methoxy-4,5-epoxymorphinan(94152-63-3)

  • 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: 94152-63-3(Hazardous Substances Data)

94152-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94152-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,5 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94152-63:
(7*9)+(6*4)+(5*1)+(4*5)+(3*2)+(2*6)+(1*3)=133
133 % 10 = 3
So 94152-63-3 is a valid CAS Registry Number.

94152-63-3Downstream Products

94152-63-3Relevant articles and documents

Synthesis of (-)-homogalanthamine from naltrexone

Yamamoto, Naoshi,Fujii, Hideaki,Imaide, Satomi,Hirayama, Shigeto,Nemoto, Toru,Inokoshi, Junji,Tomoda, Hiroshi,Nagase, Hiroshi

, p. 2257 - 2260 (2011)

Acetylcholinesterase inhibitor (-)-homogalanthamine 3 was synthesized from μ opioid antagonist naltrexone (2) in 16% total yield. The synthesis features Grob fragmentation as a key reaction, which was especially accelerated in the presence of 15-crown-5.

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