21280-30-8 Usage
Molecular structure
1-Methyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxylic acid methyl ester is a complex organic compound with a cyclohexene ring, a carboxylic acid group, and a methyl ester functional group.
Functional groups
The compound contains a carboxylic acid group (-COOH) and a methyl ester group (-COOCH3), which contribute to its chemical reactivity and properties.
Side chains
The compound has a methyl group (-CH3) and a 4-methyl-3-pentenyl group (a branched chain with a double bond) attached to the cyclohexene ring, which affects its steric properties and reactivity.
Applications
1-Methyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxylic acid methyl ester may have potential applications in organic synthesis, pharmaceuticals, or other chemical industries due to its unique structure and reactivity.
Further research
Additional studies and investigations are needed to fully understand the properties and potential uses of this compound, as its complex structure may offer new insights and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 21280-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,8 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21280-30:
(7*2)+(6*1)+(5*2)+(4*8)+(3*0)+(2*3)+(1*0)=68
68 % 10 = 8
So 21280-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O2/c1-12(2)6-5-7-13-8-10-15(3,11-9-13)14(16)17-4/h6,8H,5,7,9-11H2,1-4H3
21280-30-8Relevant articles and documents
High regioselective Diels-Alder reaction of myrcene with acrolein catalyzed by zinc-containing ionic liquids
Yin, Donghong,Li, Changzhi,Li, Biaomo,Tao, Liang,Yin, Dulin
, p. 137 - 142 (2007/10/03)
The ambient zinc-containing ionic liquids, MX-ZnCl2, functioning as both Lewis acid catalyst and green solvent, are employed for a high regioselective Diels-Alder reaction of myrcene with acrolein for the first time, where MX is either 1-butyl-3-methylimidazolium chloride (BmimCl), 1-ethyl-3-methylimidazolium bromide (EmimBr), N-butylpyridinium bromide (BPyBr), or N-ethylpyridinium bromide (EtPyBr). Compared with the analogous reaction performed over a ZnCl2 catalyst in the conventional solvent dichloromethane, higher regioselectivity of the 'para' cycloadduct and excellent yield were achieved at shorter reaction time in these ionic liquids with optimized molar compositions of MX and ZnCl2. These moisture-insensitive ionic liquids can be easily separated from reaction products after simple washing with hexane, allowing their reuse with no obvious loss in activity.
