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2,3-dimethyl-pent-1-en-3-ol is an organic compound with the molecular formula C7H14O. It is a colorless liquid with a strong, pungent odor. This chemical is a secondary alcohol with a double bond in the molecule, which gives it unique chemical properties. It is commonly used as a fragrance ingredient in the perfume industry due to its pleasant, fruity scent. Additionally, it can be found in various natural sources, such as fruits and essential oils. The compound is also known for its potential applications in the synthesis of other organic compounds and as a chemical intermediate in the pharmaceutical and chemical industries.

2004-66-2

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2004-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2004-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2004-66:
(6*2)+(5*0)+(4*0)+(3*4)+(2*6)+(1*6)=42
42 % 10 = 2
So 2004-66-2 is a valid CAS Registry Number.

2004-66-2Downstream Products

2004-66-2Relevant academic research and scientific papers

KINETICS OF THE GAS-PHASE THERMAL DECOMPOSITION OF 2,3-DIMETHYL-2,3-EPOXYPENTANE

Flowers, Michael C.,Honeyman, Malcolm R.

, p. 2179 - 2184 (2007/10/02)

In the temperature range 638-727 K 2,3-dimethyl-2,3-epoxypentane decomposes by homogeneous, unimolecular and non-radical mechanisms to give propene, propanone, but-1-ene, cis- and trans-but-1-ene, butanone, 2,2-dimethylpentan-3-one, 3,3-dimethylpentan-2-one, 2,3-dimethylpent-1-en-3-ol, 3-ethyl-2-methylbut-3-en-2-ol and 2,3-dimethylpent-3-en-2-ol as the major products.These products arise as the consequence of seven competing primary processes and the Arrhenius parameters for each of these processes are determined.The results and conclusions of this study are in accord with those of previous studies of the thermal decompositions of other alkyl-substituted oxiranes.

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