Cas 98385-72-9,(S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

98385-72-9

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Basic information

Product Name: (S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester
Synonyms: (S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester
CAS NO:98385-72-9
Molecular Formula:
Molecular Weight: 480.564
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)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(98385-72-9)
EPA Substance Registry System: (S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(98385-72-9)

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: 98385-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98385-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,8 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98385-72:
(7*9)+(6*8)+(5*3)+(4*8)+(3*5)+(2*7)+(1*2)=189
189 % 10 = 9
So 98385-72-9 is a valid CAS Registry Number.

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98385-72-9Relevant academic research and scientific papers

Synthesis and characterization of peptide-cationic steroid antibiotic conjugates

Ding, Bangwei,Taotofa, Uale,Orsak, Thomas,Chadwell, Matthew,Savage, Paul B.

, p. 3433 - 3436 (2007/10/03)

(Chemical Equation Presented) New cationic steroid antibiotics have been prepared by conjugating tripeptides to a triamino analogue of cholic acid. These compounds were synthesized on a solid phase in an indexed library that was screened for antibacterial

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