Cas 1330193-41-3,(S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide

1330193-41-3

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Basic information

Product Name: (S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide
Synonyms: (S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide
CAS NO:1330193-41-3
Molecular Formula:
Molecular Weight: 380.338
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: (S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide(1330193-41-3)
EPA Substance Registry System: (S)-N-(2-amino-3-phenylpropyl)-2,3,4,5,6-pentafluorobenzenesulfonamide(1330193-41-3)

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: 1330193-41-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1330193-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,1,9 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1330193-41:
(9*1)+(8*3)+(7*3)+(6*0)+(5*1)+(4*9)+(3*3)+(2*4)+(1*1)=113
113 % 10 = 3
So 1330193-41-3 is a valid CAS Registry Number.

1330193-41-3Upstream product

1330193-43-5 (S)-tert-butyl 1-(perfluorophenylsulfonamido)-3-phenylpropan-2-ylcarbamate

1330193-41-3Downstream Products

1330193-41-3Relevant academic research and scientific papers

Direct asymmetric aldol reactions in water with a β-aminosulfonamide organocatalyst

Miura, Tsuyoshi,Ina, Mariko,Imai, Kie,Nakashima, Kosuke,Yasaku, Yumi,Koyata, Naka,Murakami, Yasuoki,Imai, Nobuyuki,Tada, Norihiro,Itoh, Akichika

experimental part, p. 1028 - 1034 (2011/09/20)

Organocatalyst 4 promoted the direct asymmetric aldol reactions of aldehydes with ketones in brine or in the presence of water to afford the corresponding anti-aldol products in moderate to excellent yields with up to 97% ee.

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