Cas 138091-88-0,1,3,8-Triazaspiro[4.5]decan-4-one, 8-[4-(4-fluorophenyl)-4-oxobutyl]-3-[(4-methoxyphenyl)methyl]-1-phenyl-

138091-88-0

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Basic information

Product Name: 1,3,8-Triazaspiro[4.5]decan-4-one, 8-[4-(4-fluorophenyl)-4-oxobutyl]-3-[(4-methoxyphenyl)methyl]-1-phenyl-
Synonyms:
CAS NO:138091-88-0
Molecular Formula: C31H34FN3O3
Molecular Weight: 515.628
EINECS: N/A
Product Categories: N/A
Mol File: 138091-88-0.mol
Article Data: 1

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: 1,3,8-Triazaspiro[4.5]decan-4-one, 8-[4-(4-fluorophenyl)-4-oxobutyl]-3-[(4-methoxyphenyl)methyl]-1-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,8-Triazaspiro[4.5]decan-4-one, 8-[4-(4-fluorophenyl)-4-oxobutyl]-3-[(4-methoxyphenyl)methyl]-1-phenyl-(138091-88-0)
EPA Substance Registry System: 1,3,8-Triazaspiro[4.5]decan-4-one, 8-[4-(4-fluorophenyl)-4-oxobutyl]-3-[(4-methoxyphenyl)methyl]-1-phenyl-(138091-88-0)

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: 138091-88-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138091-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,0,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138091-88:
(8*1)+(7*3)+(6*8)+(5*0)+(4*9)+(3*1)+(2*8)+(1*8)=140
140 % 10 = 0
So 138091-88-0 is a valid CAS Registry Number.

138091-88-0Upstream product

749-02-0 spiperone

138091-88-0Downstream Products

138091-88-0Relevant articles and documents

Effect of N-alkylation on the affinities of analogues of spiperone for dopamine D2 and serotonin 5-HT2 receptors

Mach,Jackson,Luedtke,Ivins,Molinoff,Ehrenkaufer

, p. 423 - 430 (2007/10/02)

Two series of N-substituted spiperone analogues were prepared and evaluated in vitro to measure their affinities for dopamine D2 and serotonin 5-HT2 receptors. Substitution of the amide nitrogen with an alkyl group of five carbon uni

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