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3-Iodo-2-heptanone, also known as 3-iodooctan-2-one, is an organic compound with the chemical formula C7H15IO. It is a colorless liquid with a molecular weight of 246.10 g/mol. This ketone derivative features a seven-carbon alkyl chain with a ketone group at the second carbon and an iodine atom at the third carbon. 3-Iodo-2-heptanone is used as a synthetic intermediate in the preparation of various organic compounds, particularly in the pharmaceutical and chemical industries. It is also employed as a reagent in organic synthesis, such as in the preparation of chiral ligands and catalysts. Due to its reactivity and functional groups, it is essential to handle 2-Heptanone, 3-iodo- with care, following proper safety protocols.

2033-49-0

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2033-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2033-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2033-49:
(6*2)+(5*0)+(4*3)+(3*3)+(2*4)+(1*9)=50
50 % 10 = 0
So 2033-49-0 is a valid CAS Registry Number.

2033-49-0Relevant academic research and scientific papers

One-pot metal-free syntheses of acetophenones from styrenes through aerobic photo-oxidation and deiodination with iodine

Nobuta, Tomoya,Hirashima, Shin-Ichi,Tada, Norihiro,Miura, Tsuyoshi,Itoh, Akichika

scheme or table, p. 2576 - 2579 (2011/06/25)

A one-pot synthetic protocol of acetophenones from styrenes with molecular oxygen, visible light, and molecular iodine is reported. This procedure involves aerobic photo-oxidation and deiodination in one pot and provides the first report of metal-free direct syntheses of acetophenones from styrenes.

A New α-Iodination of Ketones Using Iodine-Ammonium Cerium(IV) Nitrate in Alcohol or Acetic Acid

Horiuchi, C. Akira,Kiji, Shinji

, p. 421 - 426 (2007/10/03)

The direct α-iodination of various ketones using iodine-ammonium cerium(IV) nitrate in acetic acid or alcohol gave the corresponding α-iodo ketones in high yields. The effect of cerium salt on the iodination of ketones, and the iodination of 5α-cholestan-3-one using several methods are also discussed. In the reaction of 3,3,5-trimethylcyclohexanone and unsymmetrical ketones, such as 2-hexanone and 2-heptanone, using methanol, ethanol, 1-propanol, and 2-propanol, the regioselective iodination product was obtained. In the case of bromination, the reaction of ketones with bromine and ammonium cerium(IV) nitrate also yielded the corresponding α-bromo ketones.

A New α-Iodination of Ketones Using Iodine-Cerium(IV) Ammonium Nitrate

Horiuchi, C. Akira,Kiji, Shinji

, p. 31 - 34 (2007/10/02)

Direct α-iodination of some ketones using iodine-cerium(IV) ammonium nitrate in acetic acid or methanol, gave the corresponding α-iodoketone in high yield.In the case of 2-pentanone, 4-methyl-2-pentanone, 2-hexanone, and 2-heptanone in methanol, the regioselective products were obtained.

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