52557-98-9 Usage
General Description
3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid is a chemical compound with a complex and rigid bicyclic structure. It is a carboxylic acid, meaning it contains a carboxyl group (-COOH) which is a key functional group in organic chemistry. The presence of two methyl groups on the bicyclic structure adds to its complexity and potential reactivity. 3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid has potential applications in pharmaceuticals, as a precursor in organic synthesis, and as a building block for creating other complex chemical structures. The unique structure and potential reactivity of 3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid make it an interesting target for further study and potential use in various chemical and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52557-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,5 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52557-98:
(7*5)+(6*2)+(5*5)+(4*5)+(3*7)+(2*9)+(1*8)=139
139 % 10 = 9
So 52557-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-10(2)7-4-3-6(5-7)8(10)9(11)12/h6-8H,3-5H2,1-2H3,(H,11,12)
52557-98-9Relevant articles and documents
Wolinsky
, p. 4150,4151 (1961)
Cobalt catalyzed oxidation of cyclic alkenes with molecular oxygen: Allylic oxidation versus double bond attack
Madhava Reddy,Punniyamurthy,Iqbal, Javed
, p. 159 - 162 (2007/10/02)
Cobalt (II) Schiff's base complex 1 and 2 exhibit a remarkable chemoselectivity during oxidation of cyclic alkenes with molecular oxygen in the presence of 2-methylpropanal. Catalyst 1 encourages the oxidation of double bond to give epoxide as the major product whereas catalyst 2 promotes mainly the allylic oxidation leading to allylic alcohols or enones.
A Simple One-pot Method for Conversion of Terminal Alkenes into Carboxylic Acids via Hydroboration
Periasamy, M.,Narayana, C.,Anitha, N.
, p. 844 - 846 (2007/10/02)
Hydroboration of terminal alkenes with NaBH4/CH3COOH followed by oxidation with aqueous chromic acids in the presence of t-butanol gives the corresponding carboxylic acids in moderate to good yields (50-75percent).
