6709-22-4 Usage
General Description
2,2,3-trimethylcyclopent-3-enecarboxylic acid is a chemical compound with a molecular formula of C9H14O2. It is a carboxylic acid derivative, with a cyclopentene ring and three methyl substituents. 2,2,3-trimethylcyclopent-3-enecarboxylic acid is used in the synthesis of other organic molecules and can also serve as a building block for pharmaceuticals and agrochemicals. Its structural arrangement and functional groups give it unique reactivity and potential applications in organic synthesis and medicinal chemistry. Furthermore, it is important to handle this compound with care, as it may have hazardous properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6709-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6709-22:
(6*6)+(5*7)+(4*0)+(3*9)+(2*2)+(1*2)=104
104 % 10 = 4
So 6709-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-6-4-5-7(8(10)11)9(6,2)3/h4,7H,5H2,1-3H3,(H,10,11)
6709-22-4Relevant articles and documents
MICROBIOLOGICAL TRANSFORMATIONS-XV; MICROBIOLOGICAL TRANSFORMATIONS OF 1-(2,2,3-TRIMETHYLCYCLOPENT-3-EN-YL)-PROPAN-2-ONE AND THEIR HOMOLOGUES BY ACREMONIUM ROSEUM s.s. GAMS 1971
Siewinski, A.,Dmochowska-Gladysz, J.,Kolek, T.,Zabza, A.,Derdzinski, K.,Nespiak, A.
, p. 2265 - 2270 (2007/10/02)
The microbiological transformations of 1-(2,2,3-trimethylcyclopent-3-en-yl)-propan-2-one (2a) and its four (2b-e) homologues by Acremonium roseum were investigated.For 2a, b and e ketones Baeyer-Villiger oxydation was predominant reaction, but ketone 2c and d were mainly hydroxylated.
