Cas 587023-38-9,(S)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one

587023-38-9

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Basic information

Product Name: (S)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one
Synonyms: (S)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one
CAS NO:587023-38-9
Molecular Formula:
Molecular Weight: 387.519
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)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one(587023-38-9)
EPA Substance Registry System: (S)-3-((1E,3E)-1-Benzyloxymethoxy-2-methyl-octa-1,3-dienyl)-4-isopropyl-oxazolidin-2-one(587023-38-9)

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: 587023-38-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 587023-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,7,0,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 587023-38:
(8*5)+(7*8)+(6*7)+(5*0)+(4*2)+(3*3)+(2*3)+(1*8)=169
169 % 10 = 9
So 587023-38-9 is a valid CAS Registry Number.

587023-38-9Upstream product

587023-38-9Downstream Products

587023-38-9Relevant academic research and scientific papers

1,3-Rearrangement of ketene-N,O-acetals

Suzuki, Tatsuo,Inui, Masaharu,Hosokawa, Seijiro,Kobayashi, Susumu

, p. 3713 - 3716 (2007/10/03)

Ketene N,O-acetals were prepared stereoselectively and submitted to a Lewis acid-mediated 1,3-rearrangement to afford C-alkylated products. The reactions proceeded in a stereoselective manner to construct a chiral quaternary carbon in high selectivity. The stereochemistry of the quaternary center was found to be opposite to that obtained by an anionic direct dienolate alkylation.

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