Cas 861445-50-3,[(S)-2-{(S)-2-[(R)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-ethoxycarbamoyl]-pyrrolidin-1-yl}-1-(4-hydroxy-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

861445-50-3

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Basic information

Product Name: [(S)-2-{(S)-2-[(R)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-ethoxycarbamoyl]-pyrrolidin-1-yl}-1-(4-hydroxy-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:861445-50-3
Molecular Formula:
Molecular Weight: 611.695
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-[(R)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-ethoxycarbamoyl]-pyrrolidin-1-yl}-1-(4-hydroxy-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-2-{(S)-2-[(R)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-ethoxycarbamoyl]-pyrrolidin-1-yl}-1-(4-hydroxy-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester(861445-50-3)
EPA Substance Registry System: [(S)-2-{(S)-2-[(R)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-ethoxycarbamoyl]-pyrrolidin-1-yl}-1-(4-hydroxy-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester(861445-50-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 861445-50-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 861445-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,4,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 861445-50:
(8*8)+(7*6)+(6*1)+(5*4)+(4*4)+(3*5)+(2*5)+(1*0)=173
173 % 10 = 3
So 861445-50-3 is a valid CAS Registry Number.

861445-50-3Upstream product

861445-50-3Downstream Products

861445-50-3Relevant academic research and scientific papers

Structure-activity relationships of novel endomorphin-2 analogues with N-O turns induced by α-aminoxy acids

Wei, Jie,Shao, Xuan,Gong, Maozhen,Zhu, Beibei,Cui, Yuxin,Gao, Yanfeng,Wang, Rui

, p. 2986 - 2989 (2007/10/03)

Endomorphin-2 (H-Tyr-Pro-Phe-Phe-NH2, EM-2) is a putative endogenous μ-opioid receptor ligand. To study the structure-activity relationship against its receptor, we introduced N-O turns into EM-2 and got the analogues with potent affinities for μ-opioid receptor. Our results indicated that N-O turn structures at the Pro2-aminoxy-Phe 3 position of EM-2 analogues played important roles for their affinities. These novel analogues with N-O turns provided a new approach to develop potent analgesics related to EM-2.

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