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2-Oxazolidinone, 3,4,5-triphenyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84327-75-3

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84327-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84327-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,2 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84327-75:
(7*8)+(6*4)+(5*3)+(4*2)+(3*7)+(2*7)+(1*5)=143
143 % 10 = 3
So 84327-75-3 is a valid CAS Registry Number.

84327-75-3Downstream Products

84327-75-3Relevant academic research and scientific papers

Cycloaddition Reaction of 2,3-Disubstituted Oxiranes with Isocyanates by Highly Activated Catalyst; Ph4SbI-Bu3SnI

Fujiwara, Masahiro,Baba, Akio,Tomohisa, Yuri,Matsuda, Haruo

, p. 1963 - 1966 (2007/10/02)

The combination of Ph4SbI and Bu3SnI proved to be a new excellent catalyst for effecting cycloaddition reaction of inactive 2,3-disubstituted oxiranes with isocyanatea under neutral conditions, yielding oxazolidinones in high yields, while either of both

Reaction of Chlorosulfonyl Isocyanate with Aziridines

Murthy, K. S. Keshava,Dhar, D. N.

, p. 1699 - 1704 (2007/10/02)

The reaction of chlorosulfonyl isocyanate (CSI) with 1,2,3-triphenylaziridine (1) and some cis- and trans-1-cyclohexyl-2-aroyl-3-phenylaziridines, 4-7 and 19-22 has been described.The cis-isomers of aziridines, 4-7, undergo a smooth reaction with CSI to give the corresponding cis-isomers of 2-chlorosulfonylimino-1,3-oxazolidines, 8-11, in good yields (65-67percent).While the trans-isomers, 19-22, gave unusal products 23-26 which have been assigned a bicylic structure, based on their physical and spectral (ir,pmr,ms) data.Plausible mechnisms have been postullated to explain the transformations.

REACTIONS OF N-PHENYL-β-AMINOALCOHOLS WITH ACETYLENIC ESTERS

Tsuge, Otohiko,Oe, Koji,Ohnishi, Toshiyuki

, p. 1609 - 1614 (2007/10/02)

erythro-1,2-Diphenyl-2-phenylaminoetanol 1 reacted with dimethyl acetylenedicarboxylate (DMAD) in refluxing benzene to give the cis-Michael adduct, whereas the same reaction in methanol at room temperature afforded a mixture of the Michael adduct and tetr

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