Cas 1194064-99-7,(+)-(2S,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide

1194064-99-7

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Basic information

Product Name: (+)-(2S,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide
Synonyms: (+)-(2S,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide
CAS NO:1194064-99-7
Molecular Formula:
Molecular Weight: 322.448
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,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(2S,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide(1194064-99-7)
EPA Substance Registry System: (+)-(2S,1'S)-2-hydroxy-N-(1-hydroxymethyl-2-methyl-propyl)-2-phenyl-3-(N,N-diethylamino)propanamide(1194064-99-7)

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: 1194064-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1194064-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,0,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1194064-99:
(9*1)+(8*1)+(7*9)+(6*4)+(5*0)+(4*6)+(3*4)+(2*9)+(1*9)=167
167 % 10 = 7
So 1194064-99-7 is a valid CAS Registry Number.

1194064-99-7Upstream product

1194064-89-5 (-)-(1S,4-S)-N,N-diethyl-1-(4-isopropyl-2-oxazolin-2-yl)-1-phenylethanolamine

1194064-99-7Downstream Products

1194064-99-7Relevant academic research and scientific papers

Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective β-lithiation

Degennaro, Leonardo,Capriati, Vito,Carlucci, Claudia,Florio, Saverio,Luisi, Renzo,Nuzzo, Irene,Cuocci, Corrado

experimental part, p. 8745 - 8755 (2009/12/28)

The synthesis of terminal oxazolinyloxiranes, even in enantioenriched form, has been performed by Darzens-type reaction of lithiated chloroalkyloxazolines with benzotriazolylmethanol (BtCH2OH) or by chloromethylation of 2-acyl-2-oxazolines. The

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