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2-((E)-4-Methyl-7-phenyl-hept-4-enyl)-[1,3]dioxolane is a complex organic compound characterized by a unique molecular structure. It features a 1,3-dioxolane ring, which is a five-membered ring containing two oxygen atoms, and an (E)-4-methyl-7-phenyl-hept-4-enyl group attached to the 2-position of the dioxolane. The (E)-4-methyl-7-phenyl-hept-4-enyl group consists of a seven-carbon chain with a methyl group at the 4th position, a phenyl group at the 7th position, and a double bond between the 4th and 5th carbons. 2-((E)-4-Methyl-7-phenyl-hept-4-enyl)-[1,3]dioxolane is known for its potential applications in the synthesis of various pharmaceuticals and fragrances, as well as its role as an intermediate in organic chemistry.

76599-50-3

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76599-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76599-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,9 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76599-50:
(7*7)+(6*6)+(5*5)+(4*9)+(3*9)+(2*5)+(1*0)=183
183 % 10 = 3
So 76599-50-3 is a valid CAS Registry Number.

76599-50-3Downstream Products

76599-50-3Relevant academic research and scientific papers

α-Haloallyllithium Species. Coupling with Alkyl Bromides

Macdonald, Timothy L.,Narayanan, Amirthalingam B.,O'Dell, Dale E.

, p. 1504 - 1506 (2007/10/02)

The regiospecific α-alkylation of in situ generated α-chloroallyllithium species with primary alkyl bromides and the synthetic utility of the derived secondary allylic chloride intermediates are described.

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