54745-74-3 Usage
Description
8-OXA-3-AZABICYCLO[3.2.1]OCTANEHYDROCHLORIDE is a chemical compound that serves as a crucial intermediate in various organic synthesis processes. It is characterized by its unique bicyclic structure and hydrochloride salt form, which contributes to its versatility in chemical reactions and applications across different industries.
Uses
Used in the Agrochemical Industry:
8-OXA-3-AZABICYCLO[3.2.1]OCTANEHYDROCHLORIDE is used as an important raw material and intermediate for the synthesis of various agrochemicals. Its role in this industry is to facilitate the development of new and improved pesticides, herbicides, and other agricultural chemicals that can enhance crop protection and yield.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, 8-OXA-3-AZABICYCLO[3.2.1]OCTANEHYDROCHLORIDE is utilized as a key intermediate in the synthesis of a wide range of pharmaceutical compounds. Its unique chemical properties allow for the creation of new drugs with potential therapeutic applications, contributing to the advancement of medical treatments and healthcare solutions.
Used in the Dyestuff Industry:
8-OXA-3-AZABICYCLO[3.2.1]OCTANEHYDROCHLORIDE also plays a significant role in the dyestuff industry, where it is employed as a vital raw material and intermediate for the production of various dyes and pigments. Its involvement in this industry helps in the development of new and innovative colorants for a diverse array of applications, including textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 54745-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54745-74:
(7*5)+(6*4)+(5*7)+(4*4)+(3*5)+(2*7)+(1*4)=143
143 % 10 = 3
So 54745-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO.ClH/c1-2-6-4-7-3-5(1)8-6;/h5-7H,1-4H2;1H
54745-74-3Relevant articles and documents
Concise syntheses of bridged morpholines
Zaytsev, Andrey V.,Pickles, James E.,Harnor, Suzannah J.,Henderson, Alistair P.,Alyasiri, Mohammed,Waddell, Paul G.,Cano, Celine,Griffin, Roger J.,Golding, Bernard T.
, p. 53955 - 53957 (2016/07/06)
Concise and practical syntheses of 8-oxa-3-aza-bicyclo[3.2.1]octane and 9-oxa-3-aza-bicyclo[3.3.1]nonane are described starting from furan-2,5-dicarboxylic acid and 4H-pyran-2,6-dicarboxylic acid, respectively, and using a solvent-free step for a key cyclisation.
8-Oxa-3-azabicyclo(3.2.1)octane analgesic compositions and method of alleviating pain in animals
-
, (2008/06/13)
Disclosed are compounds, having the following general formula, which are useful as analgesics in living animals. SPC1 Wherein R is a radical selected from the group consisting of aralkyl, aryl, aminoalkyl, arylalkanoyl, heteroaroyl, alkoxy substituted aroyl, alkenyl (C2 to C4), halogen substituted aralkyl, guanadinoalkyl, halogen substituted aroyl, alkyl substituted aroyl, halogen substituted arylalkanoyl, hexahydrobenzoyl, arylalkenoyl, o- or p-alkyl substituted phenylalkanoyl, alkyl substituted naphthylalkanoyl, alkanoyl (C3 to C20), haloalkyl substituted aroyl, alkoxy substituted aralkyl, heteroaralkyl, anilinocarbonyl, adamantanecarbonyl, arylsulfonyl, carboxyl substituted aroyl, hydroxyl substituted aroyl, alkanoyloxy substituted aroyl, arylglyoxylyl, alicyclic, arylene dicarbonyl-8-oxa-3-azabicyclo(3.2.1)octane, alkylene-8-oxa-3-azabicyclo (3.2.1)octane, alkylene dicarbonyl-8-oxa-3-azabicyclo(3.2.1)octane, and the pharmacologically acceptable acid addition salts thereof.