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3-methyl-3-hexene-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

855750-67-3

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855750-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855750-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,7,5 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 855750-67:
(8*8)+(7*5)+(6*5)+(5*7)+(4*5)+(3*0)+(2*6)+(1*7)=203
203 % 10 = 3
So 855750-67-3 is a valid CAS Registry Number.

855750-67-3Upstream product

855750-67-3Downstream Products

855750-67-3Relevant academic research and scientific papers

Rate Constants for the Reactions of Oh Radicals with 1,2,4,5- Tetramethylbenzene, Pentamethylbenzene, 2,4,5-Trimethylbenzaldehyde, 2,4,5-Trimethylphenol, and 3-Methyl-3-Hexene-2,5-Dione and Products of OH + 1,2,4,5-tetramethylbenzene

Aschmann, Sara M.,Arey, Janet,Atkinson, Roger

, p. 2556 - 2568 (2013)

Using a relative rate method, rate constants have been measured for the reactions of OH radicals with 1,2,4,5-tetramethylbenzene, pentamethylbenzene, 2,4,5-trimethylbenzaldehyde, 2,4,5-trimethylphenol and 3-methyl-3-hexene-2,5- dione at 298 ± 2 K and atmospheric pressure of air. The rate constants obtained (in units of 10-11 cm3 molecule-1 s-1) were: 1,2,4,5-tetramethylbenzene, 5.55 ± 0.34; pentamethylbenzene, 10.3 ± 0.8; 2,4,5-trimethylbenzaldehyde, 4.27 ± 0.39; 2,4,5-trimethylphenol, 9.75 ± 0.98; and 3-methyl-3-hexene-2,5-dione, 9.4 ± 1.1. The following first-generation products were identified from the OH + 1,2,4,5-tetramethylbenzene reaction in the presence of NO: biacetyl, methylglyoxal, 3-methyl-3-hexene-2,5-dione, and 2,4,5-trimethylbenzaldehyde. The measured molar formation yields for 3-methyl-3-hexene-2,5-dione and 2,4,5-trimethylbenzaldehyde were 45 ± 9% and 3.3 ± 0.7%, with that for 3-methyl-3-hexene-2,5-dione being extrapolated to low NO2 concentrations where the OH-1,2,4,5- tetramethylbenzene adducts react only with O2. Biacetyl appeared to be formed as both a first- and second-generation product, and a first-generation formation yield of 9 ± 3% was derived. The relative formation yield of methylglyoxal was ~0.8 of that for 3-methyl-3-hexene-2,5-dione, indicating that methylglyoxal and 3-methyl-3-hexene-2,5-dione are coproducts. H-atom abstraction from OH + 1,2,4,5-tetramethylbenzene is estimated to account for 3.7 ± 0.8% of the overall OH radical reaction. On the basis of the current understanding of the mechanism of the OH-aromatic adduct + O2 reaction, the observed formation of biacetyl indicates that some ipso addition of OH occurs for OH + 1,2,4,5-tetramethylbenzene.

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