Cas 134133-63-4,2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide

134133-63-4

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Basic information

Product Name: 2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide
Synonyms: 2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide
CAS NO:134133-63-4
Molecular Formula:
Molecular Weight: 479.6
EINECS: N/A
Product Categories: N/A
Mol File: 134133-63-4.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: 2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide(134133-63-4)
EPA Substance Registry System: 2-<3-<4-<4-(ethoxycarbonyl)phenyl>-1-piperazinyl>propyl>-2H-naphth<1,8-cd>isothiazole 1,1-dioxide(134133-63-4)

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: 134133-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134133-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134133-63:
(8*1)+(7*3)+(6*4)+(5*1)+(4*3)+(3*3)+(2*6)+(1*3)=94
94 % 10 = 4
So 134133-63-4 is a valid CAS Registry Number.

134133-63-4Upstream product

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134133-63-4Relevant articles and documents

Naphthosultam Derivatives: A New Class of Potent and Selective 5-HT2 Antagonists

Malleron, Jean-Luc,Comte, Marie-Therese,Gueremy, Claude,Peyronel, Jean Francois,Truchon, Alain,et al.

, p. 2477 - 2483 (2007/10/02)

A series of 2-(aminoalkyl)naphthisothiazole 1,1-dioxides was synthesized and examined in various receptor binding tests.Most compounds demonstrated high affinity for the 5-HT2 receptor with moderate to high selectivity.A member of this

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