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1H-Indole-1-carboxamide, 2,3-dihydro-2-oxo-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27284-44-2

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27284-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27284-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,8 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27284-44:
(7*2)+(6*7)+(5*2)+(4*8)+(3*4)+(2*4)+(1*4)=122
122 % 10 = 2
So 27284-44-2 is a valid CAS Registry Number.

27284-44-2Downstream Products

27284-44-2Relevant academic research and scientific papers

COMPOUND; TAUTOMER AND GEOMETRIC ISOMER THEREOF; SALT OF SAID COMPOUND, TAUTOMER, OR GEOMETRIC ISOMER; METHOD FOR MANUFACTURING SAID COMPOUND, TAUTOMER, ISOMER, OR SALT; ANTIMICROBIAL AGENT; AND ANTI-INFECTIVE DRUG

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Paragraph 0178-0179, (2015/09/23)

A compound represented by any one of General Formulas (1) to (5), a tautomer or geometric isomer thereof, or a salt thereof.

The chemistry of homophthalic acid: a new synthetic strategy for construction of substituted isocoumarin and indole skeletons

?zcan, Sevil,Balci, Metin

, p. 5531 - 5540 (2008/09/21)

Homophthalic acid was reacted with thionylchloride/DMF and chloroethylformate/NEt3 in the presence and absence of NaN3. In all cases completely different isocoumarin derivatives were obtained. These unusual isocoumarin derivatives were isolated and characterized and their formation mechanisms are discussed. The homophthalic acid monomethyl ester was converted into the corresponding isocyanate. Reaction of the isocyanate with different amines produced the urea derivatives. Base-supported condensation reactions of these products gave first an indolinone derivative, which underwent further intermolecular condensation to give substituted indole derivatives. However, when the condensation reaction was carried out in the presence of acetic anhydride, the intermolecular reactions were suppressed. This methodology opens up a new way of synthesizing of various five-membered ring substituted indole derivatives.

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