Cas 141018-43-1,{(1S,2S,4R)-1-Benzyl-5-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-hydroxy-4-[4-(2-morpholin-4-yl-ethoxy)-benzyl]-5-oxo-pentyl}-carbamic acid tert-butyl ester

141018-43-1

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Product Name: {(1S,2S,4R)-1-Benzyl-5-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-hydroxy-4-[4-(2-morpholin-4-yl-ethoxy)-benzyl]-5-oxo-pentyl}-carbamic acid tert-butyl ester
Synonyms:
CAS NO:141018-43-1
Molecular Formula:
Molecular Weight: 713.915
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: {(1S,2S,4R)-1-Benzyl-5-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-hydroxy-4-[4-(2-morpholin-4-yl-ethoxy)-benzyl]-5-oxo-pentyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(1S,2S,4R)-1-Benzyl-5-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-hydroxy-4-[4-(2-morpholin-4-yl-ethoxy)-benzyl]-5-oxo-pentyl}-carbamic acid tert-butyl ester(141018-43-1)
EPA Substance Registry System: {(1S,2S,4R)-1-Benzyl-5-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-hydroxy-4-[4-(2-morpholin-4-yl-ethoxy)-benzyl]-5-oxo-pentyl}-carbamic acid tert-butyl ester(141018-43-1)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 141018-43-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141018-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,1 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141018-43:
(8*1)+(7*4)+(6*1)+(5*0)+(4*1)+(3*8)+(2*4)+(1*3)=81
81 % 10 = 1
So 141018-43-1 is a valid CAS Registry Number.

141018-43-1Upstream product

141018-43-1Downstream Products

138483-63-3 L-689502

141018-43-1Relevant academic research and scientific papers

Highly Diastereoselective Alkylations of Chiral Amide Enolates: New Routes to Hydroxyethylene Dipeptide Isostere Inhibitors of HIV-1 Protease

Askin, D.,Wallace, M. A.,Vacca, J. P.,Reamer, R. A.,Volante, R. P.,Shinkai, I.

, p. 2771 - 2773 (2007/10/02)

The nonchelate enforced chiral amide enolates derived from 4-7 react with alkyl iodide and protected α-amino epoxide electrophiles to produce the HIV protease inhibitors 10 and 16-19 with high diastereoselectivity.

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