18088-97-6 Usage
Description
2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid is an organic compound characterized by its unique molecular structure, featuring a cyclohexene ring with three methyl groups attached at specific positions. 2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid is known for its potential applications in various industries due to its chemical properties.
Uses
Used in Chemical Synthesis:
2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid is used as an intermediate in the synthesis of various organic compounds, particularly in the production of 1,1,5,5-Tetramethyl-2-(1-methylethenyl)cyclohexane (T305630). 2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid is essential in the study of synthetic elastomers and natural rubber, where it aids in understanding the formation of cyclic oligomers in the copolymerization of isoprene with isobutylene.
Used in Rubber Industry:
In the rubber industry, 2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid plays a crucial role in the development and improvement of synthetic elastomers. Its application contributes to the enhancement of the properties of rubber materials, such as their elasticity, durability, and resistance to various environmental factors.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, the unique structure and properties of 2,4,4-Trimethyl-1-cyclohexene-1-carboxylic acid may also make it a potential candidate for pharmaceutical research. Its chemical properties could be harnessed for the development of new drugs or drug delivery systems, particularly in the field of drug synthesis and modification.
Check Digit Verification of cas no
The CAS Registry Mumber 18088-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,8 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18088-97:
(7*1)+(6*8)+(5*0)+(4*8)+(3*8)+(2*9)+(1*7)=136
136 % 10 = 6
So 18088-97-6 is a valid CAS Registry Number.
18088-97-6Relevant articles and documents
Transition metals in organic synthesis, Part 98.1 Transition metal mediated total synthesis of the potent neuronal cell protecting alkaloid (±)-lavanduquinocin
Froehner, Wolfgang,Reddy, Kethiri R.,Knoelker, Hans-Joachim
, p. 330 - 342 (2013/09/24)
An efficient total synthesis of (±)-lavanduquinocin, a potent neuronal cell protecting alkaloid from Streptomyces viridochromogenes, is reported. Key-steps are an iron-mediated one-pot construction of the carbazole framework and a nickel-mediated coupling reaction. ARKAT-USA, Inc.
An efficient synthetic method for β-cyclolavandulal and its corresponding alcohol
Oda, Mitsunori,Isobe, Atsushi,Hayashi, Masashi,Miyatake, Ryuta,Shimao, Ichiro,Kuroda, Shigeyasu
, p. 438 - 440 (2007/10/03)
3,3-Dimethylcyclohexanone (5) was efficiently converted to methyl β-cyclolavandulate (6) in 74% yield in three steps, one of which included the preparation of β-methyl α,β-unsaturated esters by coupling lithium dimethylcuprate with enol phosphates of β-ox
