10293-06-8 Usage
Description
(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is a white crystalline compound with a unique bicyclic structure and a bromine atom at the 3rd position. It is characterized by its endo configuration and the presence of three methyl groups at the 1st and 7th positions. (1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one has potential applications in various industries due to its chemical properties.
Uses
Used in Medicine:
(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is used as a pharmaceutical intermediate for the synthesis of various medicinal compounds. Its unique structure and chemical properties make it a valuable building block in the development of new drugs.
Used in the Manufacture of Camphor Derivatives:
(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is used as a key intermediate in the production of camphor derivatives. These derivatives are important in the fragrance, flavor, and pharmaceutical industries due to their unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10293-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10293-06:
(7*1)+(6*0)+(5*2)+(4*9)+(3*3)+(2*0)+(1*6)=68
68 % 10 = 8
So 10293-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H15BrO/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7H,4-5H2,1-3H3/t6-,7+,10+/m0/s1
10293-06-8Relevant articles and documents
Ranganathan,Raman
, p. 411 (1973)
New chiral cyclopalladated complexes based on the pinane and bornane imines
Kuchin,Gur'eva,Frolova,Alekseev,Zalevskaya
, p. 745 - 750 (2014/01/23)
2α-Hydroxypinan-3-one imino derivatives react with lithium tetrachloropalladate to form palladacycles, while similar bornane derivative undergo cyclopalladation only when treated with palladium acetate.
REACTIVITY OF 3-BROMOCAMPHOR AND 3-BROMOISOCAMPHANONE UNDER THE CONDITIONS OF THE RITTER REACTION
Koval'skaya, S. S.,Kozlov, N. G.,Zyryanov, V. A.
, p. 722 - 726 (2007/10/02)
The bromination of camphor and isocamphanone yield, respectively, 3-endo- and 3-exo-bromo ketones.Under the conditions of the Ritter reaction 3-bromocamphor does not react with nitriles, while 3-isocamphanone is selectively converted into the corresponding N,N'-diacyl-3-bromo-2,2-gem-diamino-5,5,6-trimethylbicycloheptanes.
ENANTIOSPECIFIC SYNTHESIS OF ESTRONE
Hutchinson, John H.,Money, Thomas
, p. 1 - 6 (2007/10/02)
Efiicient cleavage of the C(1)-C(2) bond in 9,10-dibromocamphor (3) provides a chiral intermediate (5) that can be used in a new enantiospecific synthesis of estrone.
