72597-34-3 Usage
Description
(1R)-10-CAMPHORSULFONAMIDE is a chiral compound derived from camphor, characterized by its unique (1R) configuration. It is a synthetic intermediate and an amino chiral derivative, which makes it valuable in various chemical and pharmaceutical applications due to its specific stereochemistry.
Uses
Used in Pharmaceutical Industry:
(1R)-10-CAMPHORSULFONAMIDE is used as a synthetic intermediate for the development of pharmaceutical compounds. Its chiral nature allows for the creation of enantiomerically pure drugs, which can have different biological activities and reduce potential side effects.
Used in Chemical Synthesis:
(1R)-10-CAMPHORSULFONAMIDE is used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of one enantiomer over another. This is crucial in producing enantiomerically pure compounds with desired biological properties and minimizing unwanted side effects.
Used in Asymmetric Hydroxylation:
(1R)-10-CAMPHORSULFONAMIDE is used as a chiral catalyst or ligand in asymmetric hydroxylation reactions. This application allows for the selective introduction of hydroxyl groups into molecules, which is essential in the synthesis of biologically active compounds and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 72597-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72597-34:
(7*7)+(6*2)+(5*5)+(4*9)+(3*7)+(2*3)+(1*4)=153
153 % 10 = 3
So 72597-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO3S/c1-9(2)7-3-4-10(9,8(12)5-7)6-15(11,13)14/h7H,3-6H2,1-2H3,(H2,11,13,14)/t7-,10-/m0/s1
72597-34-3Relevant articles and documents
Application of the sulfonamide functional groups as an anchor for solid phase organic synthesis (SPOS)
Beaver,Siegmund,Spear
, p. 1145 - 1148 (2007/10/03)
Sulfonyl chlorides have been found to readily couple to an amino functionalized resin. The resulting sulfonamide anchoring group is stable to a variety of reactions commonly used in SPOS. Acid induced cleavage is facile, affording functionalized sulfonamides in high yields.
