Cas 65472-78-8,2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate

65472-78-8

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Basic information

Product Name: 2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate
Synonyms: 2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate
CAS NO:65472-78-8
Molecular Formula:
Molecular Weight: 588.701
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: 2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate(65472-78-8)
EPA Substance Registry System: 2-(4-benzhydryl-1-piperazinylmethyl)-5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthalenol hydrogen fumarate(65472-78-8)

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: 65472-78-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 65472-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,7 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65472-78:
(7*6)+(6*5)+(5*4)+(4*7)+(3*2)+(2*7)+(1*8)=148
148 % 10 = 8
So 65472-78-8 is a valid CAS Registry Number.

65472-78-8Upstream product

65472-78-8Downstream Products

65472-39-1 1-Benzhydryl-4-(5,6-dimethoxy-3,4-dihydro-naphthalen-2-ylmethyl)-piperazine; hydrochloride

65472-78-8Relevant academic research and scientific papers

Synthesis and biological activities of 3-aminomethyl-1,2-dihydronaphthalene derivatives

Itoh,Miyake,Tanabe,Hirata,Oka

, p. 2006 - 2015 (2007/10/02)

A series of 3-aminomethyl-1,2-dihydronaphthalene derivatives was prepared from the corresponding 3,4-dihydro-1(2H)-naphthalenone derivatives in three steps, namely the Mannich reaction, reduction of the carbonyl group with sodium borohydride, and dehydrat

1,2-Dihydronaphthalene derivatives and pharmaceutical composition

-

, (2008/06/13)

Novel 1,2-dihydronaphthalene derivatives of the formula STR1 wherein R1 and R2, independently of each other, are hydrogen, nitro, amino, halogen, or hydroxyl which may be protected, and R3 is a piperazinyl or morpholino gr

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