Cas 1192674-19-3,(2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester

1192674-19-3

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Basic information

Product Name: (2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester
Synonyms: (2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester
CAS NO:1192674-19-3
Molecular Formula:
Molecular Weight: 264.281
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: (2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester(1192674-19-3)
EPA Substance Registry System: (2R,3R)-2-amino-3-hydroxy-3-[(5R)-phenyl-4,5-dihydroisoxazol-3-yl]-propionic acid methyl ester(1192674-19-3)

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: 1192674-19-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192674-19-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,6,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1192674-19:
(9*1)+(8*1)+(7*9)+(6*2)+(5*6)+(4*7)+(3*4)+(2*1)+(1*9)=173
173 % 10 = 3
So 1192674-19-3 is a valid CAS Registry Number.

1192674-19-3Upstream product

1192674-14-8 (R)-[(2R,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]-[(5R)-5-phenyl-4,5-dihydroisoxazol-3-yl]-methanol

1192674-19-3Downstream Products

1192674-19-3Relevant academic research and scientific papers

Enzymatic resolution of (±)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester and its transformations into polyfunctionalised amino acids and dipeptides

Cremonesi, Giuseppe,Croce, Piero Dalla,Forni, Alessandra,Gallanti, Maddalena,Gandolfi, Raffaella,La Rosa, Concetta

experimental part, p. 1940 - 1947 (2010/01/16)

Enantiomerically pure (5R)-(-)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester was obtained via enzymatic resolution of the corresponding racemic mixture using a lipase from hog pancreas (PPL). The following reduction of the ester group to the

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