Cas 122882-90-0,N-<1-(2-Phenylethyl)-4-piperidyl>-N-phenylvaleramide

122882-90-0

Post Buying Request

Basic information

Product Name: N-<1-(2-Phenylethyl)-4-piperidyl>-N-phenylvaleramide
Synonyms:
CAS NO:122882-90-0
Molecular Formula:
Molecular Weight: 364.531
EINECS: N/A
Product Categories: N/A
Mol File: 122882-90-0.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: N-<1-(2-Phenylethyl)-4-piperidyl>-N-phenylvaleramide(CAS DataBase Reference)
NIST Chemistry Reference: N-<1-(2-Phenylethyl)-4-piperidyl>-N-phenylvaleramide(122882-90-0)
EPA Substance Registry System: N-<1-(2-Phenylethyl)-4-piperidyl>-N-phenylvaleramide(122882-90-0)

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: 122882-90-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

122882-90-0 Suppliers

Recommended suppliersmore

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

122882-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122882-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122882-90:
(8*1)+(7*2)+(6*2)+(5*8)+(4*8)+(3*2)+(2*9)+(1*0)=130
130 % 10 = 0
So 122882-90-0 is a valid CAS Registry Number.

122882-90-0Upstream product

122882-90-0Downstream Products

122882-90-0Relevant articles and documents

Carbon-13 nuclear magnetic resonance spectra of fentanyl analogs

Brine,Boldt,Huang,Sawyer,Carroll

, p. 677 - 686 (2007/10/02)

Natural abundance carbon-13 chemical shifts are reported for the hydrochloride salts of fentanyl and fifteen analogs. The signals are assigned on the basis of chemical shift theory, SFORD multiplicities, signal intensities, comparisons with model compounds, and thiophene carbon-proton coupling constants. In addition to its forensic value, the data suggest that the solution conformations of the analogs are similar to that of fentanyl hydrochloride.