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p-hydroxybenzaldehyde azine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41097-49-8

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41097-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41097-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,9 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41097-49:
(7*4)+(6*1)+(5*0)+(4*9)+(3*7)+(2*4)+(1*9)=108
108 % 10 = 8
So 41097-49-8 is a valid CAS Registry Number.

41097-49-8Relevant academic research and scientific papers

The Reaction of Hydrazine with α-Cyanocinnamate Esters: A Caveat

Erdman, Paul J.,Gosse, Jimmy L.,Jacobson, Jamey A.,Lewis, David E.

, p. 1163 - 1171 (2004)

α-Cyanocinnamate esters react with hydrazine to give initial products of conjugate addition that then undergo a fragmentation to give the azine of the carbonyl precursor to the starting ester, rather than intramolecular aminolysis to give the pyrazolidino

Rapid, chemoselective and facile synthesis of azines by hydrazine/I2

Nanjundaswamy,Pasha

, p. 3417 - 3420 (2008/02/13)

We report the reaction of hydrazine hydrate with carbonyl compounds in the presence of molecular iodine at 0-10°C, which affords symmetrical azines in excellent yields in 1 to 4 min without any adverse effect on other substituents. The reactions are rapid and chemoselective, afford excellent yields, and have high-purity products. The workup procedure is environmentally benign and does not require solvent extraction. Copyright Taylor & Francis Group, LLC.

Selective protection of carbonyl compounds as azines and their facile regeneration

Nanjundaswamy,Pasha

, p. 3161 - 3165 (2007/10/03)

Carbonyl compounds with freshly prepared hydrazinium formate successfully yielded the corresponding azines in excellent yields. In turn, azines were deprotected to the corresponding carbonyls using triethylammonium chlorochromate chemoselectively. Copyright Taylor & Francis Group, LLC.

Aspects of acyclic azine chemistry -- I. The effect of structure and solvents on the electronic absorption spectra of benzaldazine, o-, m- and p-hydroxybenzaldazines

Okafor, E. Chukwuemeka

, p. 207 - 212 (2007/10/02)

The electronic absorption spectra of benzaldazine, o-, m-, and p-hydroxybenzaldazines have been separately examined in various solvents (20 solvents and solvent mixtures).The observed three groups of bands designated as α (200-225 nm), β (289-307 nm) and γ (352-375 nm) are attributed to ?* IAu IAg) are out-of-plane (Ξ) polarized while all ?* IBu IAg) are in plane (x,y) polarized.In the rationalization of data, the theory of resonance has been employed where deemed useful.The shifts of bands with solvents have been traced.

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