Cas 155512-41-7,1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan

155512-41-7

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Basic information

Product Name: 1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan
Synonyms: 1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan
CAS NO:155512-41-7
Molecular Formula:
Molecular Weight: 519.643
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: 1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan(CAS DataBase Reference)
NIST Chemistry Reference: 1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan(155512-41-7)
EPA Substance Registry System: 1'-(o-aminobenzyl)-17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,14-dihydroxyindolo<2',3':6,7>morphinan(155512-41-7)

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: 155512-41-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155512-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155512-41:
(8*1)+(7*5)+(6*5)+(5*5)+(4*1)+(3*2)+(2*4)+(1*1)=117
117 % 10 = 7
So 155512-41-7 is a valid CAS Registry Number.

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155512-41-7Relevant academic research and scientific papers

N-Benzylnaltrindoles as Long-Acting δ-Opioid Receptor Antagonist

Korlipara, V. L.,Takemori, A. E.,Portoghese, P. S.

, p. 1882 - 1885 (1994)

The indolic nitrogen of the δ-opioid receptor antagonist, naltrindole (1), was derivatized with benzyl or substituted benzyl to afford a series (2-9) that retained δ-opioid receptor antagonist activity and selectivity in vitro.The two most potent members

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