Cas 161990-12-1,2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester

161990-12-1

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Basic information

Product Name: 2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester
Synonyms: 2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester
CAS NO:161990-12-1
Molecular Formula:
Molecular Weight: 615.723
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: 2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester(161990-12-1)
EPA Substance Registry System: 2-((3S,5S,6R)-4-Benzyloxycarbonyl-2-oxo-5,6-diphenyl-morpholin-3-ylmethyl)-malonic acid di-tert-butyl ester(161990-12-1)

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: 161990-12-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161990-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,9 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 161990-12:
(8*1)+(7*6)+(6*1)+(5*9)+(4*9)+(3*0)+(2*1)+(1*2)=141
141 % 10 = 1
So 161990-12-1 is a valid CAS Registry Number.

161990-12-1Upstream product

161990-12-1Downstream Products

161990-12-1Relevant academic research and scientific papers

Chiral Synthesis of L-γ-Carboxylgutamic Acid (L-Gla)

Schuerman, Marla A.,Keverline, Kathryn I.,Hiskey, Richard G.

, p. 825 - 828 (1995)

A two step synthesis involving the use of a chiral template, benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholine-carboxylate (5a), provides orthogonally protected L-Gla (9) in 60percent overall yield (>99percent ee), with no resolution required.

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