Cas 1394249-59-2,3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

1394249-59-2

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Basic information

Product Name: 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one
Synonyms: 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one
CAS NO:1394249-59-2
Molecular Formula:
Molecular Weight: 283.37
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-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one(1394249-59-2)
EPA Substance Registry System: 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one(1394249-59-2)

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: 1394249-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394249-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,2,4 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1394249-59:
(9*1)+(8*3)+(7*9)+(6*4)+(5*2)+(4*4)+(3*9)+(2*5)+(1*9)=192
192 % 10 = 2
So 1394249-59-2 is a valid CAS Registry Number.

1394249-59-2Upstream product

37580-42-0 (E)-2-methyl-1-phenyl-1,3-butadiene

1394249-59-2Downstream Products

1394249-59-2Relevant academic research and scientific papers

Axially chiral triazoloisoquinolin-3-ylidene ligands in gold(I)-catalyzed asymmetric intermolecular (4 + 2) cycloadditions of allenamides and dienes

Francos, Javier,Grande-Carmona, Francisca,Faustino, Helio,Iglesias-Sigueenza, Javier,Diez, Elena,Alonso, Isaac,Fernandez, Rosario,Lassaletta, Jose M.,Lopez, Fernando,Mascarenas, Jose L.

supporting information, p. 14322 - 14325 (2012/10/29)

The first highly enantioselective intermolecular (4 + 2) cycloaddition between allenes and dienes is reported. The reaction provides good yields of optically active cyclohexenes featuring diverse substitution patterns and up to three stereocenters. Key to

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