Cas 1329627-28-2,(S)-N,2-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide

1329627-28-2

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Basic information

Product Name: (S)-N,2-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide
Synonyms: (S)-N,2-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide
CAS NO:1329627-28-2
Molecular Formula:
Molecular Weight: 322.495
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-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N,2-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide(1329627-28-2)
EPA Substance Registry System: (S)-N,2-dimethyl-N-((S)-2-phenyl-1-(thiazol-2-yl)ethyl)propane-2-sulfinamide(1329627-28-2)

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: 1329627-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1329627-28-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,9,6,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1329627-28:
(9*1)+(8*3)+(7*2)+(6*9)+(5*6)+(4*2)+(3*7)+(2*2)+(1*8)=172
172 % 10 = 2
So 1329627-28-2 is a valid CAS Registry Number.

1329627-28-2Upstream product

1329627-28-2Downstream Products

386743-16-4 (S)-N-methyl-2-phenyl-1-(thiazol-2-yl)ethanamine

1329627-28-2Relevant academic research and scientific papers

Efficient total synthesis of dysidenin, dysidin, and barbamide

Ilardi, Elizabeth A.,Zakarian, Armen

supporting information; experimental part, p. 2260 - 2263 (2012/06/30)

The total syntheses of three trichloroleucine-derived marine natural products-dysidenin, dysidin, and barbamide-capitalized on a practical and highly diastereoselective ruthenium catalyzed radical chloroalkylation of N-acyloxazolidinones as the key step. Copyright

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