Cas 1097642-41-5,(S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine hydrochloride

1097642-41-5

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Basic information

Product Name: (S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine hydrochloride
Synonyms:
CAS NO:1097642-41-5
Molecular Formula:
Molecular Weight: 383.748
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: (S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine hydrochloride(1097642-41-5)
EPA Substance Registry System: (S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine hydrochloride(1097642-41-5)

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: 1097642-41-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1097642-41-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,6,4 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1097642-41:
(9*1)+(8*0)+(7*9)+(6*7)+(5*6)+(4*4)+(3*2)+(2*4)+(1*1)=175
175 % 10 = 5
So 1097642-41-5 is a valid CAS Registry Number.

1097642-41-5Upstream product

1097775-19-3 (S)-4-(3,4-dichlorophenyl)-4-(1H-indol-4-yl)-N-methylbutan-1-amine

1097642-41-5Downstream Products

1097642-41-5Relevant academic research and scientific papers

1-Naphthyl and 4-indolyl arylalkylamines as selective monoamine reuptake inhibitors

Manning, James R.,Sexton, Tammy,Childers, Steven R.,Davies, Huw M.L.

supporting information; experimental part, p. 58 - 61 (2009/05/26)

A series of enantiomerically pure 1-naphthyl and 4-indolyl arylalkylamines were prepared and evaluated for their binding affinities to the monoamine transporters. The two series of enantiomers displayed considerable differences in binding selectivity betw

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