Cas 1198053-75-6,(1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate

1198053-75-6

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Basic information

Product Name: (1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate
Synonyms: (1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate
CAS NO:1198053-75-6
Molecular Formula:
Molecular Weight: 405.945
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: (1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate(1198053-75-6)
EPA Substance Registry System: (1S,2R)-1-(3-chlorophenyl)-1-((R)-1,1-dimethylethylsulfinamido)but-3-en-2-yl benzoate(1198053-75-6)

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: 1198053-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198053-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,0,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1198053-75:
(9*1)+(8*1)+(7*9)+(6*8)+(5*0)+(4*5)+(3*3)+(2*7)+(1*5)=176
176 % 10 = 6
So 1198053-75-6 is a valid CAS Registry Number.

1198053-75-6Upstream product

1198053-75-6Downstream Products

1198053-96-1 C₁₉H₁₈ClNO₃

1198053-75-6Relevant academic research and scientific papers

Highly efficient asymmetric synthesis of vinylic amino alcohols by znpromoted benzoyloxyallylation of chiral N-tert-butanesulfinyl imines: Facile and rapid access to (-)-cytoxazone

Liu, Min,Sun, Xing-Wen,Xu, Ming-Hua,Lin, Guo-Qiang

experimental part, p. 10217 - 10224 (2010/04/05)

An efficient and convenient α-hydroxyallylation approach for the asymmetric synthesis of a variety of βamino-α-vinyl alcohols has been successfully developed. A wide range of vinylic amino alcohol derivatives could be obtained in very good yields and with

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