Cas 177544-15-9,3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ<sup>6</sup>-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide

177544-15-9

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Basic information

Product Name: 3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide
Synonyms: 3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide
CAS NO:177544-15-9
Molecular Formula:
Molecular Weight: 398.399
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: 3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide(177544-15-9)
EPA Substance Registry System: 3-Methyl-5-oxo-4-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-2,5-dihydro-pyrazole-1-carboxylic acid phenylamide(177544-15-9)

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: 177544-15-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 177544-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 177544-15:
(8*1)+(7*7)+(6*7)+(5*5)+(4*4)+(3*4)+(2*1)+(1*5)=159
159 % 10 = 9
So 177544-15-9 is a valid CAS Registry Number.

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177544-15-9Relevant academic research and scientific papers

Synthesis of 1-substituted and 1-unsubstituted 4-sulfonamido-1H-pyrazol-5(2H)-ones

Arcadi,Attanasi,De Crescentini,Rossi,Serra-Zanetti

, p. 533 - 536 (1996)

4-Sulfonamido-1H-pyrazol-5(2H)-ones bearing different substituent groups on the nitrogen atom in position 1 were easily obtained by reaction of conjugated azoalkenes with sulfonamides under mild conditions. 1-Unsubstituted title compounds were smoothly obtained by solvolytic cleavage of the substituent groups in methanol under reflux.

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