Cas 1332355-98-2,N-((2S,3R)-1-(2-(1H-indazole-3-carbonyl)hydrazinyl)-3-hydroxy-1-oxobutan-2-yl)benzenesulfonamide

1332355-98-2

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Basic information

Product Name: N-((2S,3R)-1-(2-(1H-indazole-3-carbonyl)hydrazinyl)-3-hydroxy-1-oxobutan-2-yl)benzenesulfonamide
Synonyms:
CAS NO:1332355-98-2
Molecular Formula:
Molecular Weight: 417.445
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: N-((2S,3R)-1-(2-(1H-indazole-3-carbonyl)hydrazinyl)-3-hydroxy-1-oxobutan-2-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2S,3R)-1-(2-(1H-indazole-3-carbonyl)hydrazinyl)-3-hydroxy-1-oxobutan-2-yl)benzenesulfonamide(1332355-98-2)
EPA Substance Registry System: N-((2S,3R)-1-(2-(1H-indazole-3-carbonyl)hydrazinyl)-3-hydroxy-1-oxobutan-2-yl)benzenesulfonamide(1332355-98-2)

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: 1332355-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332355-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,3,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1332355-98:
(9*1)+(8*3)+(7*3)+(6*2)+(5*3)+(4*5)+(3*5)+(2*9)+(1*8)=142
142 % 10 = 2
So 1332355-98-2 is a valid CAS Registry Number.

1332355-98-2Upstream product

93474-55-6 (2S,3R)-3-hydroxy-2-(phenylsulfonamido)butanoic acid

1332355-98-2Downstream Products

1332355-98-2Relevant academic research and scientific papers

Design, synthesis and in vitro biochemical activity of novel amino acid sulfonohydrazide inhibitors of MurC

Frlan, Rok,Kovas, Andreja,Blanot, Didier,Gobec, Stanislav,Pecar, Slavko,Obreza, Ales

, p. 295 - 310 (2012/04/23)

Mur ligases are essential enzymes involved in the cytoplasmic steps of peptidoglycan synthesis which remain attractive, yet unexploited targets. In order to develop new antibacterial agents, we have designed a series of new MurC and MurD inhibitors bearin

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