Cas 133042-79-2,17-(cyclopropylmethyl)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan

133042-79-2

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Basic information

Product Name: 17-(cyclopropylmethyl)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan
Synonyms: 17-(cyclopropylmethyl)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan
CAS NO:133042-79-2
Molecular Formula:
Molecular Weight: 419.521
EINECS: N/A
Product Categories: N/A

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)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan(CAS DataBase Reference)
NIST Chemistry Reference: 17-(cyclopropylmethyl)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan(133042-79-2)
EPA Substance Registry System: 17-(cyclopropylmethyl)-4,5α-epoxy-6-phenyl-3,6,14β-trihydroxymorphinan(133042-79-2)

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: 133042-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133042-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,4 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133042-79:
(8*1)+(7*3)+(6*3)+(5*0)+(4*4)+(3*2)+(2*7)+(1*9)=92
92 % 10 = 2
So 133042-79-2 is a valid CAS Registry Number.

133042-79-2Upstream product

133042-79-2Downstream Products

133042-78-1 17-(cyclopropylmethyl)-6,7-didehydro-3,14β-dihydroxy-4,5α-epoxy-6-phenylmorphinan

133042-79-2Relevant academic research and scientific papers

Role of Spacer and Address Components in Peptidomimetic δ Opioid Receptor Antagonists Related to Naltrindole

Portoghese, P. S.,Nagase, H.,MaloneyHuss, K. E.,Lin, C.-E.,Takemori, A. E.

, p. 1715 - 1720 (1991)

A series of heterocyclic analogues 2-5 related to naltrindole (1) (NTI) and 6-arylnaltrexone derivatives 6-8 were synthesized in order to determine the role of the spacer and the address moieties in conferring δ opioid receptor antagonist activity.The ben

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