Cas 215929-72-9,(R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one

215929-72-9

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Basic information

Product Name: (R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one
Synonyms: (R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one
CAS NO:215929-72-9
Molecular Formula:
Molecular Weight: 424.31
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: (R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one(215929-72-9)
EPA Substance Registry System: (R)-2-[Bis-(2-chloro-ethyl)-amino]-1-methyl-3-((S)-1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,3,2]diazaphosphinin-4-one(215929-72-9)

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: 215929-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 215929-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,9,2 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 215929-72:
(8*2)+(7*1)+(6*5)+(5*9)+(4*2)+(3*9)+(2*7)+(1*2)=149
149 % 10 = 9
So 215929-72-9 is a valid CAS Registry Number.

215929-72-9Upstream product

215929-72-9Downstream Products

215929-72-9Relevant academic research and scientific papers

Synthesis of chiral bis-(2-chloroethyl)amino-substituted 1,3,2σ3λ3 (or σ4λ5)benzodiazaphosphorinones; resolution, oxidation reactions and X-ray structure determinations of individual enantiomers

Fei, Zhaofu,Neda, Ion,Thoennessen, Holger,Jones, Peter G.,Schmutzler, Reinhard

, p. 1 - 23 (2007/10/03)

The chiral N-methyl-N′-(1-phenylethyl)-substituted anthranilamides R-(+)-3 (RC-enantiomer) and S-( - )-3 (SC-enantiomer) were formed by reaction of N-methylisatoic anhydride, 1, with R-( + )-and S-( - )-1-phenylethylamine, R-( + )-2

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