Cas 1228159-84-9,8-phenyl-5-(phenylsulfonyl)-8H-[1,2,5]oxadiazolo[3,4-g]-indazole 3-oxide

1228159-84-9

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Basic information

Product Name: 8-phenyl-5-(phenylsulfonyl)-8H-[1,2,5]oxadiazolo[3,4-g]-indazole 3-oxide
Synonyms:
CAS NO:1228159-84-9
Molecular Formula:
Molecular Weight: 392.395
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: 8-phenyl-5-(phenylsulfonyl)-8H-[1,2,5]oxadiazolo[3,4-g]-indazole 3-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 8-phenyl-5-(phenylsulfonyl)-8H-[1,2,5]oxadiazolo[3,4-g]-indazole 3-oxide(1228159-84-9)
EPA Substance Registry System: 8-phenyl-5-(phenylsulfonyl)-8H-[1,2,5]oxadiazolo[3,4-g]-indazole 3-oxide(1228159-84-9)

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: 1228159-84-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1228159-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,1,5 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1228159-84:
(9*1)+(8*2)+(7*2)+(6*8)+(5*1)+(4*5)+(3*9)+(2*8)+(1*4)=159
159 % 10 = 9
So 1228159-84-9 is a valid CAS Registry Number.

1228159-84-9Upstream product

1228159-82-7 7-azido-6-nitro-1-phenyl-4-(phenylsulfonyl)-1H-indazole

1228159-84-9Downstream Products

1228159-84-9Relevant academic research and scientific papers

Synthesis of polycyclic fused heterocycles based on 4,6-dinitro-1-phenyl- 1H-indazole

Bastrakov,Starosotnikov,Kachala,Glukhov,Shevelev

experimental part, p. 414 - 420 (2010/07/08)

Tricyclic heteroaromatic systems of the furoxan, vic-triazole, imidazole, and pyrazine series containing the annulated indazole fragment were synthesized based on substituted aminoindazoles prepared by the functionalization of 4-R-6-nitro-1-phenylindazole

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