Cas 24775-76-6,N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride

24775-76-6

Basic information

Product Name: N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride
Synonyms: 4-Anilino-1-phenethylpiperidine dihydrochloride;N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride;4-Anilino-N-phenethyl-4-piperidone;N-Phenyl-1-(2-phenethyl)piperidin-4-amine dihydrochloride;N-Phenyl-1-(2-phenylethyl)-4-piperidimine hydrochloride;N-phenyl-1-(2-phenylethyl)piperidin-4-amine:dihydrochloride
CAS NO:24775-76-6
Molecular Formula: C19H24N2.2(HCl)
Molecular Weight: 316.8682
EINECS: N/A
Product Categories: N/A
Mol File: 24775-76-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride(24775-76-6)
EPA Substance Registry System: N-Phenyl-1-(2-phenylethyl)-4-piperidinamine hydrochloride(24775-76-6)

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: 24775-76-6(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

24775-76-6 Suppliers

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

24775-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24775-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,7 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24775-76:
(7*2)+(6*4)+(5*7)+(4*7)+(3*5)+(2*7)+(1*6)=136
136 % 10 = 6
So 24775-76-6 is a valid CAS Registry Number.

24775-76-6Upstream product

24775-76-6Downstream Products

437-38-7 N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]propanamide

24775-76-6Relevant academic research and scientific papers

Methods For Preparing Fentanyl And Fentanyl Intermediates

-

Paragraph 0042; 0043; 0044; 0045; 0046; 0047; 0048, (2013/11/05)

A method and an intermediate are provided for preparing fentanyl. Aniline and 1-phenylethyl-4-piperidone are reacted with a borane complex, in a lower C1-C4 alcoholic solvent, in the presence of an alkanoic acid. The reaction mixture is then treated with a hydrohalic acid to precipitate 4-anilino-N-phenethyl-4-piperidine (ANPP) as the bis-hydrohalide salt in high yield and purity. This ANPP salt may be directly treated with propionyl halide to produce fentanyl, or the ANPP salt may be converted to the free base of ANPP and similarly treated with propionyl halide to produce fentanyl.