Cas 91622-85-4,(3aS,4R,6S,6aS)-4,6-Dimethoxy-3-phenyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole

91622-85-4

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Basic information

Product Name: (3aS,4R,6S,6aS)-4,6-Dimethoxy-3-phenyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole
Synonyms:
CAS NO:91622-85-4
Molecular Formula:
Molecular Weight: 247.294
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: (3aS,4R,6S,6aS)-4,6-Dimethoxy-3-phenyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,6S,6aS)-4,6-Dimethoxy-3-phenyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole(91622-85-4)
EPA Substance Registry System: (3aS,4R,6S,6aS)-4,6-Dimethoxy-3-phenyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole(91622-85-4)

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: 91622-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91622-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91622-85:
(7*9)+(6*1)+(5*6)+(4*2)+(3*2)+(2*8)+(1*5)=134
134 % 10 = 4
So 91622-85-4 is a valid CAS Registry Number.

91622-85-4Upstream product

91622-85-4Downstream Products

91622-85-4Relevant academic research and scientific papers

STEREOSELECTIVITIES OF BENZONITRILE OXIDE CYCLOADDITIONS TO CIS DISUBSTITUTED CYCLOPENTENES AND DIHYDROFURANS

Caramella, P.,Albini, Marinone F.,Vitali, D.,Rondan, Nelson G.,Wu, Yun-Dong,et al.

, p. 1875 - 1878 (2007/10/02)

Benzonitrile oxide cycloadds preferentially anti to the substituents of cis-3,5-di-X-cyclopentenes, where X= OMe, OAc, OCOPh, Br, Cl, and OH.Higher stereoselectivities are found for cis-2,5-di-X-2,5-dihydrofurans.The origins of these selectivities, and contrasts with acyclic and cyclobutene analogs, are described.

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