Cas 76107-48-7,N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide

76107-48-7

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Basic information

Product Name: N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide
Synonyms: N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide
CAS NO:76107-48-7
Molecular Formula:
Molecular Weight: 366.503
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: N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide(CAS DataBase Reference)
NIST Chemistry Reference: N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide(76107-48-7)
EPA Substance Registry System: N-phenyl-N-<1-<2-(2-methoxyphenyl)-ethyl>-4-piperidinyl>-propanamide(76107-48-7)

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: 76107-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76107-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76107-48:
(7*7)+(6*6)+(5*1)+(4*0)+(3*7)+(2*4)+(1*8)=127
127 % 10 = 7
So 76107-48-7 is a valid CAS Registry Number.

76107-48-7Upstream product

76107-48-7Downstream Products

76107-51-2 N-{1-[2-(2-Hydroxy-phenyl)-ethyl]-piperidin-4-yl}-N-phenyl-propionamide

76107-48-7Relevant academic research and scientific papers

Structure and receptor interactions of morphinomimetics. Part I. Hydroxy and methoxy derivatives of fentanyl and some morphine analogues

Lobbezoo,Soudijn,Van Wijngaarden

, p. 357 - 361 (2007/10/02)

The opiate receptor affinity of a number of fentanyl derivatives was determined by in vitro receptor binding studies and compared with that of morphine-like structures. The phenolic OH groups in morphine and in a benzomorphan derivative have a strong affi

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