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(3Z)-2,4-dimethylhex-3-ene, an organic compound with the chemical formula C8H16, is a colorless liquid characterized by a fruity odor. As an alkene, it features a carbon-carbon double bond and is distinguished by the specific arrangement of its carbon atoms, which is reflected in its name. (3Z)-2,4-dimethylhex-3-ene is naturally present in fruits and vegetables and is known for its applications beyond its natural occurrence.

37682-92-1

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37682-92-1 Usage

Uses

Used in Flavor and Fragrance Industry:
(3Z)-2,4-dimethylhex-3-ene serves as a flavoring agent in the food and beverage industry, leveraging its fruity aroma to enhance the sensory experience of various products. Its natural occurrence in fruits and vegetables adds to its appeal as a flavoring agent, ensuring a familiar and authentic taste.
Used in Perfumery:
In the production of fragrances and perfumes, (3Z)-2,4-dimethylhex-3-ene is utilized for its distinctive fruity scent, contributing to the creation of complex and pleasant olfactory compositions.
Used in Chemical Synthesis:
(3Z)-2,4-dimethylhex-3-ene also plays a role as a starting material in the synthesis of various other organic compounds within the chemical industry. Its reactive carbon-carbon double bond makes it a versatile building block for the development of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 37682-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,8 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37682-92:
(7*3)+(6*7)+(5*6)+(4*8)+(3*2)+(2*9)+(1*2)=151
151 % 10 = 1
So 37682-92-1 is a valid CAS Registry Number.

37682-92-1Upstream product

37682-92-1Downstream Products

37682-92-1Relevant academic research and scientific papers

Chemo- and diastereoselectivity in the dimethyldioxirane oxidation of 2,3-dihydro-4H-1-benzothiopyran-4-ones and 4H-1-benzothiopyran-4-ones. Unusual reactivity of 4H-1-benzothiopyran-4-one 1-oxides1

Patonay,Adam,Levai,Koever,Nemeth,Peters,Peters

, p. 2275 - 2280 (2007/10/03)

The oxidation of the 1-thiochromanones 1-3 by dimethyldioxirane (DMD) produced the corresponding sulfoxides 4-6 or sulfones 7-9; their relative amounts depended on the amount of oxidant used. A low diastereoselectivity was observed in the sulfoxidation of

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