Cas 948832-29-9,diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate

948832-29-9

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Basic information

Product Name: diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate
Synonyms: diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate
CAS NO:948832-29-9
Molecular Formula:
Molecular Weight: 421.452
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: diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate(948832-29-9)
EPA Substance Registry System: diethyl (3R,5S)-5-(mesyloxymethyl)-2-[(R)-1-phenylethyl]isoxazolidinyl-3-phosphonate(948832-29-9)

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: 948832-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 948832-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,8,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 948832-29:
(8*9)+(7*4)+(6*8)+(5*8)+(4*3)+(3*2)+(2*2)+(1*9)=219
219 % 10 = 9
So 948832-29-9 is a valid CAS Registry Number.

948832-29-9Upstream product

948832-29-9Downstream Products

948832-29-9Relevant academic research and scientific papers

Enantiomerically pure phosphonate analogues of cis- and trans-4-hydroxyprolines

Piotrowska, Dorota G.,Glowacka, Iwona E.

, p. 1351 - 1363 (2008/02/08)

All the enantiomers of O,O-diethyl 4-hydroxypyrrolidinyl-2-phosphonates, phosphonate analogues of cis- and trans-4-hydroxyprolines, have been obtained for the first time. The synthetic strategy involved 1,3-dipolar cycloaddition of (R)- and (S)-N-(1-pheny

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