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"Z,E-5-(4-methyl-3-cyclohexenyl)-3-methyl-2,4-pentadienoic acid" is a complex organic compound characterized by a pentadienoic acid structure with a cyclohexenyl group attached at the 5th position. The molecule features a Z,E configuration, indicating the arrangement of double bonds, with the Z configuration referring to the cis arrangement of substituents on the double bond and the E configuration referring to the trans arrangement. The cyclohexenyl group is a 4-methyl substituted cyclohexene ring, and the pentadienoic acid backbone has a 3-methyl substitution. Z,E-5-(4-methyl-3-cyclohexenyl)-3-methyl-2,4-pentadienoic acid is known for its potential applications in the synthesis of various pharmaceuticals and natural products, particularly those involving the cyclohexane ring system. Its unique structure and functional groups make it a subject of interest in organic chemistry and drug development.

75091-86-0

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75091-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75091-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,9 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75091-86:
(7*7)+(6*5)+(5*0)+(4*9)+(3*1)+(2*8)+(1*6)=140
140 % 10 = 0
So 75091-86-0 is a valid CAS Registry Number.

75091-86-0Downstream Products

75091-86-0Relevant academic research and scientific papers

SYNTHESIS OF SOME ANALOGS OF ABSCISIC ACID FROM 3-CYCLOHEXENE-1-CARBALDEHYDE AND ITS METHYL HOMOLOGS

Gramenitskaya, V. N.,Koz'mina, E. A.,Golovkina, L. S.,Vul'fson, N. S.

, p. 1690 - 1695 (2007/10/02)

The E,E and Z,E isomers of 5-substituted 3-methyl-2,4-pentanedioic acids were synthesized from 3-cyclohexene-1-carbaldehyde and its methyl homologs.The possibilities of their production by the Reformatsky and Wittig reactions or by condensation of substituted 3-cyclohexene-1-carbaldehydes with diethyl β-methylglutaconate were investigated.It was shown that the last path makes it possible to obtain the Z,E isomers preferentially.

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