Cas 803683-48-9,3-Oxazolidinecarboxamide, N-(2,2-dimethyl-1-oxo-4-pentenyl)-2,2-dimethyl-4-(phenylmethyl)-, (4S)-

803683-48-9

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Basic information

Product Name: 3-Oxazolidinecarboxamide, N-(2,2-dimethyl-1-oxo-4-pentenyl)-2,2-dimethyl-4-(phenylmethyl)-, (4S)-
Synonyms:
CAS NO:803683-48-9
Molecular Formula: C20H28N2O3
Molecular Weight: 344.454
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: 3-Oxazolidinecarboxamide, N-(2,2-dimethyl-1-oxo-4-pentenyl)-2,2-dimethyl-4-(phenylmethyl)-, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxazolidinecarboxamide, N-(2,2-dimethyl-1-oxo-4-pentenyl)-2,2-dimethyl-4-(phenylmethyl)-, (4S)-(803683-48-9)
EPA Substance Registry System: 3-Oxazolidinecarboxamide, N-(2,2-dimethyl-1-oxo-4-pentenyl)-2,2-dimethyl-4-(phenylmethyl)-, (4S)-(803683-48-9)

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: 803683-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 803683-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,3,6,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 803683-48:
(8*8)+(7*0)+(6*3)+(5*6)+(4*8)+(3*3)+(2*4)+(1*8)=169
169 % 10 = 9
So 803683-48-9 is a valid CAS Registry Number.

803683-48-9Upstream product

803683-48-9Downstream Products

803683-54-7 (R)-1-((S)-4-Benzyl-2,2-dimethyl-oxazolidine-3-carbonyl)-5-iodomethyl-3,3-dimethyl-pyrrolidin-2-one

803683-48-9Relevant academic research and scientific papers

Asymmetric iodolactamization induced by chiral oxazolidine auxiliary

Shen, Meihua,Li, Chaozhong

, p. 7906 - 7909 (2004)

Asymmetric iodolactamization reactions of unsaturated amides with oxazolidines as the chiral auxiliaries were investigated. With (4S)-4-((2R)-2-butyl)-2,2-dimethyloxazolidine as the auxiliary and LiH as the base, a number of unsaturated amides underwent i

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