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CAS 10293-10-4

:

(1R,3S,4S,7R)-3-Bromo-7-(bromomethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-one

Description:
The chemical substance known as (1R,3S,4S,7R)-3-Bromo-7-(bromomethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-one, with the CAS number 10293-10-4, is a bicyclic compound characterized by its complex stereochemistry and the presence of bromine substituents. This compound features a bicyclo[2.2.1]heptane framework, which is a saturated hydrocarbon structure consisting of two bridged cyclopropane rings. The specific stereochemical configuration indicated by the (1R,3S,4S,7R) notation suggests that it has multiple chiral centers, contributing to its potential biological activity and specificity in interactions. The presence of bromine atoms introduces significant reactivity, making it a candidate for various chemical transformations. Additionally, the ketone functional group (indicated by the "2-one" suffix) suggests that it may exhibit properties typical of carbonyl compounds, such as reactivity in nucleophilic addition reactions. Overall, this compound's unique structure and functional groups may render it of interest in synthetic organic chemistry and potentially in medicinal chemistry for the development of bioactive molecules.
Formula:C10H14Br2O
InChI:InChI=1S/C10H14Br2O/c1-9-4-3-6(7(12)8(9)13)10(9,2)5-11/h6-7H,3-5H2,1-2H3/t6-,7+,9+,10-/m1/s1
InChI key:InChIKey=DCDNKSJBRIJYEC-GOZTYBTRSA-N
SMILES:C(Br)[C@@]1(C)[C@]2(C)C(=O)[C@@H](Br)[C@]1(CC2)[H]
Synonyms:
  • (+)-3,9-Dibromocamphor
  • (+)-endo-3,9-Dibromocamphor
  • (1R,3S,4S,7R)-3-Bromo-7-(bromomethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-one
  • (1S,4R)-3-bromo-7-(bromomethyl)-1,7-dimethyl-norbornan-2-one
  • 2-Bornanone, 3,8-dibromo-, endo-(+)-
  • 3-Bromo-7-(Bromomethyl)-1,7-Dimethylbicyclo[2.2.1]Heptan-2-One
  • Bicyclo[2.2.1]heptan-2-one, 3-bromo-7-(bromomethyl)-1,7-dimethyl-, (1R,3S,4S,7R)-
  • Bicyclo[2.2.1]heptan-2-one, 3-bromo-7-(bromomethyl)-1,7-dimethyl-, (endo,anti)-(+)-
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