Cas 950782-94-2,(3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate

950782-94-2

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Basic information

Product Name: (3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate
Synonyms: (3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate
CAS NO:950782-94-2
Molecular Formula:
Molecular Weight: 353.398
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: (3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate(950782-94-2)
EPA Substance Registry System: (3R,4S,5S)-diisopropyl (1,5-dimethyl-2-oxo-4-phenylpyrrolidin-3-yl)phosphonate(950782-94-2)

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: 950782-94-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 950782-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,7,8 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 950782-94:
(8*9)+(7*5)+(6*0)+(5*7)+(4*8)+(3*2)+(2*9)+(1*4)=202
202 % 10 = 2
So 950782-94-2 is a valid CAS Registry Number.

950782-94-2Upstream product

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950782-94-2Relevant academic research and scientific papers

Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates: Synthesis and applications of α-phosphono lactams

Bower, John F.,Williams, Andrew J.,Woodward, Hannah L.,Szeto, Peter,Lawrence, Ron M.,Gallagher, Timothy

, p. 2636 - 2644 (2007)

Five and six ring α-phosphono lactams 14-20 are available by reaction of 1,2- and 1,3-cyclic sulfamidates respectively with enolates derived from ethyl dialkylphosphonoacetates 3 and 4. Subsequent Wadsworth-Emmons olefination provides the enantiomerically

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