Cas 1986-83-0,2-amino-4-chloro-5-fluorobenzenesulfonamide

1986-83-0

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Basic information

Product Name: 2-amino-4-chloro-5-fluorobenzenesulfonamide
Synonyms: 2-amino-4-chloro-5-fluorobenzenesulfonamide
CAS NO:1986-83-0
Molecular Formula:
Molecular Weight: 224.643
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-amino-4-chloro-5-fluorobenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-chloro-5-fluorobenzenesulfonamide(1986-83-0)
EPA Substance Registry System: 2-amino-4-chloro-5-fluorobenzenesulfonamide(1986-83-0)

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: 1986-83-0(Hazardous Substances Data)

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1986-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1986-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1986-83:
(6*1)+(5*9)+(4*8)+(3*6)+(2*8)+(1*3)=120
120 % 10 = 0
So 1986-83-0 is a valid CAS Registry Number.

1986-83-0Upstream product

367-21-5 3-chloro-4-fluorophenylamine

1986-83-0Downstream Products

1034331-56-0 (E)-N-(5-chloro-4-fluoro-2-sulfamoyl-phenyl)-3-naphthalen-2-yl-acrylamide

1986-83-0Relevant academic research and scientific papers

3-Alkylamino-4H-1,2,4-benzothiadiazine 1,1-dioxides as ATP-sensitive potassium channel openers: Effect of 6,7-disubstitution on potency and tissue selectivity

De Tullio, Pascal,Boverie, Stéphane,Becker, Bénédicte,Antoine, Marie-Hélène,Nguyen, Quynh-Anh,Francotte, Pierre,Counerotte, Stéphane,Sebille, Sophie,Pirotte, Bernard,Lebrun, Philippe

, p. 4990 - 5000 (2007/10/03)

A series of 6,7-disubstituted 4H-1,2,4-benzothiadiazine 1,1-dioxides bearing a short alkylamino side chain in the 3-position were synthesized. These compounds were tested on rat pancreatic islets and on rat aorta rings. In vitro data indicated that in mos

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