Cas 864724-82-3,N-(3-iodo-4-(2-trimethylsilanyl-ethoxy)-1-methyl-1H-7-indazolyl)-4-methoxybenzene sulfonamide

864724-82-3

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Basic information

Product Name: N-(3-iodo-4-(2-trimethylsilanyl-ethoxy)-1-methyl-1H-7-indazolyl)-4-methoxybenzene sulfonamide
Synonyms:
CAS NO:864724-82-3
Molecular Formula:
Molecular Weight: 559.5
EINECS: N/A
Product Categories: N/A
Mol File: 864724-82-3.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: N-(3-iodo-4-(2-trimethylsilanyl-ethoxy)-1-methyl-1H-7-indazolyl)-4-methoxybenzene sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-iodo-4-(2-trimethylsilanyl-ethoxy)-1-methyl-1H-7-indazolyl)-4-methoxybenzene sulfonamide(864724-82-3)
EPA Substance Registry System: N-(3-iodo-4-(2-trimethylsilanyl-ethoxy)-1-methyl-1H-7-indazolyl)-4-methoxybenzene sulfonamide(864724-82-3)

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: 864724-82-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 864724-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,7,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 864724-82:
(8*8)+(7*6)+(6*4)+(5*7)+(4*2)+(3*4)+(2*8)+(1*2)=203
203 % 10 = 3
So 864724-82-3 is a valid CAS Registry Number.

864724-82-3Upstream product

864724-82-3Downstream Products

864724-82-3Relevant articles and documents

New and efficient synthesis of bi- and trisubstituted indazoles

Bouissane, Latifa,El Kazzouli, Sa?d,Léger, Jean-Michel,Jarry, Christian,Rakib, El Mostapha,Khouili, Mostafa,Guillaumet, Gérald

, p. 8218 - 8225 (2005)

In this paper, the synthesis of bi- and trisubstituted indazoles was described. 4-Alkoxy-7-aminoprotected-indazole or 7-aminoprotected-indazole derivatives were prepared selectively using SnCl2 in alcohol or SnCl2 in ethyl acetate, r

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