Cas 1610892-95-9,N-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide

1610892-95-9

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Basic information

Product Name: N-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide
Synonyms: N-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide
CAS NO:1610892-95-9
Molecular Formula:
Molecular Weight: 612.748
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-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide(CAS DataBase Reference)
NIST Chemistry Reference: N-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide(1610892-95-9)
EPA Substance Registry System: N-acetylamino-N'-di-(tert-butyloxycarbonyl)guanidinohexanoic acid [2-(4-sulfamoylphenyl)ethyl]amide(1610892-95-9)

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: 1610892-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1610892-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,8,9 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1610892-95:
(9*1)+(8*6)+(7*1)+(6*0)+(5*8)+(4*9)+(3*2)+(2*9)+(1*5)=169
169 % 10 = 9
So 1610892-95-9 is a valid CAS Registry Number.

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1610892-95-9Relevant academic research and scientific papers

Sulfonamides with potent inhibitory action and selectivity against the α-carbonic anhydrase from Vibrio cholerae

Ceruso, Mariangela,Del Prete, Sonia,Alothman, Zeid,Capasso, Clemente,Supuran, Claudiu T.

, p. 826 - 830 (2014)

By using N-α-acetyl-l-lysine or GABA scaffolds and the conversion of the terminal amino group to the guanidine one, benzenesulfonamides incorporating water solubilizing moieties were synthesized. The new compounds were medium potency inhibitors of the cyt

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