Cas 1582229-99-9,(2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate

1582229-99-9

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Basic information

Product Name: (2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate
Synonyms: (2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate
CAS NO:1582229-99-9
Molecular Formula:
Molecular Weight: 389.516
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: (2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate(1582229-99-9)
EPA Substance Registry System: (2S,3R)-methyl N-((S)-tert-butylsulfinyl)-3-hydroxy-3-(3-methoxyphenyl)-2-phenyl-propanimidate(1582229-99-9)

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: 1582229-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1582229-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,2,2,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1582229-99:
(9*1)+(8*5)+(7*8)+(6*2)+(5*2)+(4*2)+(3*9)+(2*9)+(1*9)=189
189 % 10 = 9
So 1582229-99-9 is a valid CAS Registry Number.

1582229-99-9Upstream product

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1582229-99-9Relevant academic research and scientific papers

Sulfinylimidates as chiral amide equivalents for irreversible, asymmetric aldol reactions

Bartrum, Hannah E.,Viceriat, Audrey,Carret, Sebastien,Poisson, Jean-Francois

, p. 1972 - 1975 (2014)

A highly selective N-sulfinylimidate aldolization has been developed under mildly basic conditions leading to diastereopure products of high synthetic potential. The innate reversibility of this aldolization was suppressed by the use of titanium as the Lewis acid. An application of this methodology via the synthesis of a potential neurotransmitter reuptake inhibitor is illustrated.

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