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2-Ethyl-3-methoxy-3-phenyl-2,3-dihydro-isoindol-1-one is a complex organic compound with the molecular formula C18H19NO2. It is a derivative of isoindol-1-one, which is a heterocyclic compound containing a benzene ring fused to a dihydroisoindole ring. The structure of 2-ethyl-3-methoxy-3-phenyl-2,3-dihydro-isoindol-1-one is characterized by an ethyl group at the 2-position, a methoxy group at the 3-position, and a phenyl group also at the 3-position. 2-ethyl-3-methoxy-3-phenyl-2,3-dihydro-isoindol-1-one is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex molecules, given its structural features. It may also be of interest in materials science for its potential properties, such as its reactivity or stability. The specific applications and properties of 2-ethyl-3-methoxy-3-phenyl-2,3-dihydro-isoindol-1-one would depend on its chemical behavior and the context in which it is used.

733-85-7

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733-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 733-85-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 733-85:
(5*7)+(4*3)+(3*3)+(2*8)+(1*5)=77
77 % 10 = 7
So 733-85-7 is a valid CAS Registry Number.

733-85-7Relevant academic research and scientific papers

Facile synthesis of non-nucleoside compounds starting from a-chlorocarbenium ions and isocyanates as potential hiv-1 reverse transcriptase inhibitors

Hamed, Atef A.,Zeid, Ibrahim F.,Manaa, Alaa A.

experimental part, p. 555 - 564 (2010/03/03)

Chloro(phenyl)carbenium hexachloroantimonate salts react with isocyanates to afford either isoindolium (1) or benzoxazinium salts (2). Addition of one equivalent of alcohol to 2 led, after hydrolysis with aq. NaOH, to the formation of benzoxazin-2-ones 3. Treatment with a large excess of alcohol transformed the salts 1 and 2 to the corresponding isoindol-1-ones 11 and the isocyanates 5, respectively. Reaction of 5 with primary amines furnished the urea derivatives 6 in good yield. The biological activity of 6a - o against HIV-1 was determined.

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