Cas 198779-12-3,(1S(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide

198779-12-3

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Basic information

Product Name: (1S(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide
Synonyms: (1S(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide
CAS NO:198779-12-3
Molecular Formula:
Molecular Weight: 239.29
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(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide(CAS DataBase Reference)
NIST Chemistry Reference: (1S(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide(198779-12-3)
EPA Substance Registry System: (1S(R),2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-fluoropropionamide(198779-12-3)

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: 198779-12-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 198779-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,7,7 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 198779-12:
(8*1)+(7*9)+(6*8)+(5*7)+(4*7)+(3*9)+(2*1)+(1*2)=213
213 % 10 = 3
So 198779-12-3 is a valid CAS Registry Number.

198779-12-3Upstream product

198779-12-3Downstream Products

198779-12-3Relevant academic research and scientific papers

Practical methodology for the asymmetric synthesis of organofluorine compounds

Myers, Andrew G.,McKinstry, Lydia,Barbay, Joseph K.,Gleason, James L.

, p. 1335 - 1338 (2007/10/03)

Pseudoephedrine α-fluoroacetamide (1), a nonvolatile, crystalline solid, is alkylated efficiently and with high diastereoselectivity with reactive alkyl halides. The alkylation products can be hydrolyzed under mild basic conditions to form α-fluoro carboxylates with high enantiomeric enrichment.

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