Cas 867171-45-7,(3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one

867171-45-7

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Basic information

Product Name: (3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one
Synonyms: (3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one
CAS NO:867171-45-7
Molecular Formula:
Molecular Weight: 418.533
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: (3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one(867171-45-7)
EPA Substance Registry System: (3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropylisoxazolidin-5-one(867171-45-7)

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: 867171-45-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867171-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,1,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 867171-45:
(8*8)+(7*6)+(6*7)+(5*1)+(4*7)+(3*1)+(2*4)+(1*5)=197
197 % 10 = 7
So 867171-45-7 is a valid CAS Registry Number.

867171-45-7Upstream product

74-88-4 methyl iodide

867171-45-7Downstream Products

867171-62-8 (3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-isopropylazetidin-2-one

867171-45-7Relevant academic research and scientific papers

Asymmetric inverse electron-demand 1,3-dipolar cycloaddition of ynolates with a chiral nitrone derived from L-serine leading to β-amino acid derivatives

Shindo, Mitsuru,Ohtsuki, Keiko,Shishido, Kozo

, p. 2821 - 2831 (2007/10/03)

Asymmetric 1,3-dipolar cycloaddition of lithium ynolates with a nitrone derived from Garner's aldehyde is described. The cycloadducts, 5-isoxazolidinones, were obtained in good yields with high diastereoselectivity. Alkylation of the intermediates, the 5-

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