5932-53-6 Usage
Description
(+/-)-exo-6-Hydroxytropinone is an organic compound that exists in two enantiomeric forms, which are mirror images of each other. It is characterized by its off-white to beige crystalline structure and is known for its chemical properties that make it a valuable reagent in the synthesis of certain compounds.
Uses
Used in Pharmaceutical Industry:
(+/-)-exo-6-Hydroxytropinone is used as a reagent for the preparation of racemic scopolamine, which is a tropane alkaloid. This alkaloid has various applications in the pharmaceutical industry, particularly as a medication to treat conditions such as motion sickness, nausea, and vomiting. Additionally, it is used as a preoperative medication to induce sedation, amnesia, and reduce anxiety in patients.
The use of (+/-)-exo-6-Hydroxytropinone in the synthesis of racemic scopolamine highlights its importance in the development of medications that can alleviate various symptoms and improve the quality of life for patients. Its role as a reagent in the pharmaceutical industry underscores the significance of its chemical properties and its potential for further research and development in the field of drug synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 5932-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5932-53:
(6*5)+(5*9)+(4*3)+(3*2)+(2*5)+(1*3)=106
106 % 10 = 6
So 5932-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-9-5-2-6(10)4-7(9)8(11)3-5/h5,7-8,11H,2-4H2,1H3/p+1/t5-,7+,8+/m1/s1
5932-53-6Relevant articles and documents
Novel 6-substituted 8-azabicyclo [3.2.1.] octanes as potential opiate agonists and antagonists
Dewar,Parfitt,Sheh
, p. 228 - 234 (2007/10/02)
Reaction of 8-methyl-8-azabicyclo[3.2.1]octan-6-one (tropan-6-one) with aryl magnesium halides selectively yields 6β-aryl-6α-hydroxy-8-methyl-8-azabicyclo[3.2.1]octanes (6β-aryl-6α-hydroxytropanes). 1H nmr studies supporting the assignment are presented, together with 13C data of these alcohols and various derivatives prepared as potential agonists and antagonists of opiate receptors. The results from 1H nmr studies of 6-hydroxytropan-3-one, the synthesis of which was reported in 1952, support the assigned 6β-hydroxy stereochemistry.