Cas 88284-84-8,(1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid

88284-84-8

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Basic information

Product Name: (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid
Synonyms:
CAS NO:88284-84-8
Molecular Formula:
Molecular Weight: 613.754
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: (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid(88284-84-8)
EPA Substance Registry System: (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid(88284-84-8)

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: 88284-84-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88284-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,8 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88284-84:
(7*8)+(6*8)+(5*2)+(4*8)+(3*4)+(2*8)+(1*4)=178
178 % 10 = 8
So 88284-84-8 is a valid CAS Registry Number.

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88284-84-8Relevant 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

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