Cas 1016259-43-0,17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan

1016259-43-0

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Basic information

Product Name: 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan
Synonyms: 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan
CAS NO:1016259-43-0
Molecular Formula:
Molecular Weight: 460.573
EINECS: N/A
Product Categories: N/A
Mol File: 1016259-43-0.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan(CAS DataBase Reference)
NIST Chemistry Reference: 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan(1016259-43-0)
EPA Substance Registry System: 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-(phenylacetamido)morphinan(1016259-43-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1016259-43-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1016259-43-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,2,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1016259-43:
(9*1)+(8*0)+(7*1)+(6*6)+(5*2)+(4*5)+(3*9)+(2*4)+(1*3)=120
120 % 10 = 0
So 1016259-43-0 is a valid CAS Registry Number.

1016259-43-0Upstream product

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1016259-43-0Relevant articles and documents

Synthesis and biological evaluation of α- and β-6-amido derivatives of 17-cyclopropylmethyl-3,14β-dihydroxy-4, 5α- epoxymorphinan: Potential alcohol-cessation agents

Ghirmai, Senait,Azar, Marc R.,Polgar, Wilma E.,Berzetei-Gurske, Ilona,Cashman, John R.

, p. 1913 - 1924 (2008/12/21)

Substituted aryl and aliphatic amide analogues of 6-naltrexamine were synthesized and used to characterize the binding to and functional activity of human μ-, δ-, and κ-opioid receptors. Competition binding assays showed 11-25 and 27-31 bound to the μ (K

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