Cas 150494-36-3,1-<1(S)-(tert-butoxycarbonyl)-2-methylpropyl>-5-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-2,3,6,7-tetrahydro-1H-azepin-2-one

150494-36-3

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Basic information

Product Name: 1-<1(S)-(tert-butoxycarbonyl)-2-methylpropyl>-5-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-2,3,6,7-tetrahydro-1H-azepin-2-one
Synonyms:
CAS NO:150494-36-3
Molecular Formula:
Molecular Weight: 549.826
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: 1-<1(S)-(tert-butoxycarbonyl)-2-methylpropyl>-5-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-2,3,6,7-tetrahydro-1H-azepin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-<1(S)-(tert-butoxycarbonyl)-2-methylpropyl>-5-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-2,3,6,7-tetrahydro-1H-azepin-2-one(150494-36-3)
EPA Substance Registry System: 1-<1(S)-(tert-butoxycarbonyl)-2-methylpropyl>-5-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-2,3,6,7-tetrahydro-1H-azepin-2-one(150494-36-3)

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: 150494-36-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150494-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150494-36:
(8*1)+(7*5)+(6*0)+(5*4)+(4*9)+(3*4)+(2*3)+(1*6)=123
123 % 10 = 3
So 150494-36-3 is a valid CAS Registry Number.

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150494-36-3Relevant academic research and scientific papers

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of γ-turn mimetics into a model substrate

Newlander,Callahan,Moore,Tomaszek Jr.,Huffman

, p. 2321 - 2331 (1993)

C7 mimetics, designed to lock three amino acid residues of a peptide chain into a γ-turn conformation, were introduced sequentially between the P3 to P2' positions of a model HIV-1 protease substrate I (resulting in compou

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