Cas 179083-47-7,(S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester

179083-47-7

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Basic information

Product Name: (S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester
Synonyms:
CAS NO:179083-47-7
Molecular Formula:
Molecular Weight: 583.725
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: (S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester(179083-47-7)
EPA Substance Registry System: (S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester(179083-47-7)

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: 179083-47-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179083-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,8 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 179083-47:
(8*1)+(7*7)+(6*9)+(5*0)+(4*8)+(3*3)+(2*4)+(1*7)=167
167 % 10 = 7
So 179083-47-7 is a valid CAS Registry Number.

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179083-47-7Relevant academic research and scientific papers

Conversion of acyclic nonpeptide CCK antagonists into CCK agonists

Hirst, Gavin C.,Queen, Kennedy L.,Sugg, Elizabeth E.,Willson, Timothy M.

, p. 511 - 514 (2007/10/03)

The CCK antagonists RP 69758 and (R)-lorglumide were converted into CCK agonists by the introduction of an N-isopropylanilide agonist 'trigger'. The common structural features of these ligands suggest that nonpeptide agonists and antagonists bind to a common site in the CCK receptor.

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