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40739-73-9

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40739-73-9 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 32, p. 4260, 1984 DOI: 10.1248/cpb.32.4260

Check Digit Verification of cas no

The CAS Registry Mumber 40739-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40739-73:
(7*4)+(6*0)+(5*7)+(4*3)+(3*9)+(2*7)+(1*3)=119
119 % 10 = 9
So 40739-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5NO4/c10-6-3-1-2-5-4-7(9(11)12)13-8(5)6/h1-4,10H

40739-73-9Downstream Products

40739-73-9Relevant articles and documents

Reactions of Salicylaldehydes with Bromonitromethane

Ohishi, Yoshitaka,Doi, Yoshio,Nakanishi, Teruo

, p. 4260 - 4270 (2007/10/02)

Various salicylaldehydes were treated with bromonitromethane in the presence of an inorganic base to give 2-nitrobenzofuran derivatives, and the reaction mechanisms were investigated.The most remarkable feature of the reactions is that 3-hydroxysalicylaldehyde (1k) alone among various hydroxysalicylaldehydes (1b, k, n, r) gave 2-nitro-7-hydroxybenzofuran in good yield.Bromonitromethane reacted with salicylaldehydes at the aldehyde group exclusively to give 1-(2-hydroxyphenyl)-2-bromo-2-nitroethanols (14), followed by cyclization to produce mixtures consisting of cis- and trans-2-nitro-3-hydroxy-2,3-dihydrobenzofurans (8a, b; 9a, b; 10a, b).The stereochemistry of these products is discussed on the basis of the spectral data and chemical reactivities.The intermediates, 2,3-dihydrobenzofurans, underwent dehydration smoothly to give 2-nitrobenzofurans.Keywords - bromonitromethane; salicylaldehyde derivative; ring closure; 2-nitrobenzofuran derivative; cis-2-nitro-3-hydroxy-2,3-dihydrobenzofuran derivative; trans-2-nitro-3-hydroxy-2,3-dihydrobenzofuran derivative; 13C-NMR; stereochemistry; reaction mechanism

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