Cas 1567841-00-2,(-)-di-(1S,2R,5S)-menthyl (R<SUB>S</SUB>,S<SUB>C</SUB>)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate

1567841-00-2

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Basic information

Product Name: (-)-di-(1S,2R,5S)-menthyl (R_S,S_C)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate
Synonyms: (-)-di-(1S,2R,5S)-menthyl (R_S,S_C)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate
CAS NO:1567841-00-2
Molecular Formula:
Molecular Weight: 601.831
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: (-)-di-(1S,2R,5S)-menthyl (R_S,S_C)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate(CAS DataBase Reference)
NIST Chemistry Reference: (-)-di-(1S,2R,5S)-menthyl (R_S,S_C)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate(1567841-00-2)
EPA Substance Registry System: (-)-di-(1S,2R,5S)-menthyl (R_S,S_C)-1-phenyl-1-(p-tolylsulfinylamino)-methanephosphonate(1567841-00-2)

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: 1567841-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1567841-00-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,8,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1567841-00:
(9*1)+(8*5)+(7*6)+(6*7)+(5*8)+(4*4)+(3*1)+(2*0)+(1*0)=192
192 % 10 = 2
So 1567841-00-2 is a valid CAS Registry Number.

1567841-00-2Upstream product

1567841-00-2Downstream Products

37714-06-0 (S)-amino(phenyl)methylphosphonic acid

1567841-00-2Relevant academic research and scientific papers

Double asymmetric induction in the synthesis of enantiomeric α-aminophosphonic acids mediated by sulfinimines

Lyzwa, Piotr

, p. 15 - 19 (2014)

A double asymmetric induction in the synthesis of α-aminophosphonic acids is described. It involves the nucleophilic addition of anions of enantiomeric dimenthyl phosphites to both (+)-(S)- and (-)-(R)-enantiomers of N-(p-tolylsulfinyl)benzaldimine and subsequent acidic hydrolysis of the adducts formed. The match and mismatch effects were observed.

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