Cas 1284299-35-9,diethyl (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate

1284299-35-9

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Basic information

Product Name: diethyl (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate
Synonyms: diethyl (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate
CAS NO:1284299-35-9
Molecular Formula:
Molecular Weight: 373.386
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 (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate(1284299-35-9)
EPA Substance Registry System: diethyl (1S,2S)-3-acetoxy-1-hydroxy-2-[(R)-1-phenylethylamino]propylphosphonate(1284299-35-9)

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: 1284299-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1284299-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,2,9 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1284299-35:
(9*1)+(8*2)+(7*8)+(6*4)+(5*2)+(4*9)+(3*9)+(2*3)+(1*5)=189
189 % 10 = 9
So 1284299-35-9 is a valid CAS Registry Number.

1284299-35-9Upstream product

64-19-7 acetic acid

1284299-35-9Downstream Products

1284299-39-3 diethyl (2R,3S)-3-acetoxymethyl-1-[(R)-1-phenylethyl]aziridin-2-yl-2-phosphonate

1284299-35-9Relevant academic research and scientific papers

Synthesis of four stereoisomers of protected 1,2-epiimino-3- hydroxypropylphosphonates

Wroblewski, Andrzej E.,Drozd, Joanna

, p. 200 - 206 (2011)

Enantiomerically pure protected 1,2-epiimino-3-hydroxypropylphosphonates were synthesised from hydroxy-1-{[(R)- or (S)-1-phenylethyl]aziridin-2-yl} methylphosphonates via regioselective ring opening with acetic acid followed by a stereospecific intramolec

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