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2,4-dimethyl-3-heptene is an organic compound belonging to the alkene class, characterized by the presence of a carbon-carbon double bond. It has a molecular formula of C9H18 and a molecular weight of 126.24 g/mol. The structure of 2,4-dimethyl-3-heptene consists of a seven-carbon chain with two methyl groups attached to the second and fourth carbon atoms, respectively, and the double bond located between the third and fourth carbon atoms. 2,4-dimethyl-3-heptene is a colorless liquid with a pungent odor and is insoluble in water but soluble in organic solvents. It is commonly used as a chemical intermediate in the synthesis of various chemicals, such as fragrances, pharmaceuticals, and polymers. Due to its reactive nature, 2,4-dimethyl-3-heptene should be handled with care, as it can undergo various chemical reactions, including polymerization, oxidation, and addition reactions.

3074-66-6

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3074-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3074-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3074-66:
(6*3)+(5*0)+(4*7)+(3*4)+(2*6)+(1*6)=76
76 % 10 = 6
So 3074-66-6 is a valid CAS Registry Number.

3074-66-6Upstream product

3074-66-6Downstream Products

3074-66-6Relevant academic research and scientific papers

Reactions of Propene on Zeolite HY Catalyst Studied by in Situ Variable-Temperature Solid-State Nuclear Magnetic Resonance Spectroscopy

Haw, James F.,Richardson, Benny R.,Oshiro, Irene S.,Lazo, Noel D.,Speed, James A.

, p. 2052 - 2058 (2007/10/02)

The oligomerization reactions of propene on zeolite catalyst HY have been studied in detail by in situ variable-temperature 13C solid-state NMR with cross polarization (CP) and magic-angle spinning (MAS).Propene is shown to be highly mobile in the zeolite at temperature far below the onset of chemical reactivity.Alkoxy species formed between protonated alkenes and zeolite framework oxygens are found to be important long-lived intermediates in the reactions.Simple secondary or tertiary carbocations either do not exist as free ions in the zeolite at low temperature or are so transient that they are not detected by NMR even at temperatures as low as 163 K.There is, however, evidence for long-lived alkyl-substituted cyclopentenyl carbocations, which are formed as free ions in the zeolite at room temperature.These carbocations do not form until all of the propene is consumed and hence do not play a significant role in the oligomerization reactions.A detailed reaction mechanism is proposed to account for all of the experimental observations.Novel experimental techniques are introduced which will be applicable to the study of many highly reactive catalyst/adsorbate systems.

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