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1166387-58-1

6beta-tosylnaltrexamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1166387-58-1 Structure

  • Basic information

    1. Product Name: 6beta-tosylnaltrexamate
    2. Synonyms: 6beta-tosylnaltrexamate
    3. CAS NO:1166387-58-1
    4. Molecular Formula:
    5. Molecular Weight: 497.612
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1166387-58-1.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: 6beta-tosylnaltrexamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6beta-tosylnaltrexamate(1166387-58-1)
    11. EPA Substance Registry System: 6beta-tosylnaltrexamate(1166387-58-1)

  • 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: 1166387-58-1(Hazardous Substances Data)

1166387-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1166387-58-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,6,3,8 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1166387-58:
(9*1)+(8*1)+(7*6)+(6*6)+(5*3)+(4*8)+(3*7)+(2*5)+(1*8)=181
181 % 10 = 1
So 1166387-58-1 is a valid CAS Registry Number.

1166387-58-1Downstream Products

1166387-58-1Relevant articles and documents

Design, synthesis, and characterization of 6β-naltrexol analogs, and their selectivity for in vitro opioid receptor subtypes

Pelotte, Andrea L.,Smith, Ryan M.,Ayestas, Mario,Dersch, Christina M.,Bilsky, Edward J.,Rothman, Richard B.,Deveau, Amy M.

, p. 2811 - 2814 (2009)

Since the mu opioid receptor (MOR) is known to be involved in the therapeutically relevant pathways leading to the manifestation of pain and addiction, we are currently studying the specific structural characteristics that promote antagonism at the MOR. T

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