Cas 344741-74-8,2-(4-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol

344741-74-8

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Basic information

Product Name: 2-(4-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol
Synonyms: 2-(4-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol
CAS NO:344741-74-8
Molecular Formula:
Molecular Weight: 420.595
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-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol(344741-74-8)
EPA Substance Registry System: 2-(4-Benzyl-piperidin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol(344741-74-8)

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: 344741-74-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 344741-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,7,4 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 344741-74:
(8*3)+(7*4)+(6*4)+(5*7)+(4*4)+(3*1)+(2*7)+(1*4)=148
148 % 10 = 8
So 344741-74-8 is a valid CAS Registry Number.

344741-74-8Upstream product

344741-74-8Downstream Products

88290-10-2 4-[6-(4-Benzyl-piperidin-1-ylmethyl)-7,8-dihydro-naphthalen-2-yl]-morpholine; hydrochloride

344741-74-8Relevant 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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