Cas 194551-76-3,(2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester

194551-76-3

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Basic information

Product Name: (2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester
Synonyms: (2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester
CAS NO:194551-76-3
Molecular Formula:
Molecular Weight: 487.639
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: (2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester(194551-76-3)
EPA Substance Registry System: (2S,5S)-6-Benzyloxy-5-dibenzylamino-2-isopropyl-4-oxo-hexanoic acid methyl ester(194551-76-3)

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: 194551-76-3(Hazardous Substances Data)

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194551-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194551-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,5,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 194551-76:
(8*1)+(7*9)+(6*4)+(5*5)+(4*5)+(3*1)+(2*7)+(1*6)=163
163 % 10 = 3
So 194551-76-3 is a valid CAS Registry Number.

194551-76-3Upstream product

148773-91-5 (R)-1-(methoxycarbonyl)-2-methylpropyl trifluoromethanesulfonate

194551-76-3Downstream Products

194551-76-3Relevant academic research and scientific papers

A stereocontrolled, convergent synthesis of hydroxyethylene dipeptide isosteres

Tao, Junhua,Hoffman, Robert V.

, p. 6240 - 6244 (1997)

A simple, convergent, and stereoselective synthesis of hydroxyethylene dipeptide isosteres 1 and 2 from scalemic α-hydroxy esters has been developed. The method is short (six steps), efficient (?15-25% overall), and highly diastereoselective (86-94% de) and enantioselective (>95% ee).

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