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1,2-dibromo-1-(4-acetoxy-3-methoxyphenyl)-propane is a complex organic chemical compound with the molecular formula C12H15Br2O4. It is a colorless to pale yellow liquid with a molecular weight of 380.06 g/mol. 1,2-dibromo-1-(4-acetoxy-3-methoxyphenyl)-propane is characterized by the presence of two bromine atoms attached to the first and second carbon atoms of a propane chain, with a 4-acetoxy-3-methoxyphenyl group attached to the terminal carbon. The 4-acetoxy-3-methoxyphenyl group consists of a benzene ring with a methoxy group at the 3-position and an acetoxy group at the 4-position. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and herbicides. Due to its complex structure and potential applications, it is an important compound in the field of organic chemistry and chemical engineering.

1215-30-1

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1215-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1215-30:
(6*1)+(5*2)+(4*1)+(3*5)+(2*3)+(1*0)=41
41 % 10 = 1
So 1215-30-1 is a valid CAS Registry Number.

1215-30-1Relevant academic research and scientific papers

Synthesis of Coniferyl and Dihydroconiferyl Derivatives Using Radical Bromination with N-Bromosuccinimide as the Key Step

Lindeberg, Otto

, p. 15 - 20 (2007/10/02)

Coniferyl and dihydroconiferyl derivatives have been synthesized by reacting bromides, obtained from allylic and benzylic brominations using N-bromosuccinimide (NBS), with appropriate nucleophiles.For instance, NBS bromination of eugenol acetate, followed by replacement of bromine by an acetoxy group and subsequent reduction with lithium aluminium hydride, afforded coniferyl alcohol in 65percent overall yield.Due to the availability of the starting materials (eugenol and isoeugenol) and the good overall yields obtained, these synthetic routes compete well with other methods of preparation.

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