192775-97-6 Usage
Description
2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE is a complex organic compound characterized by the presence of a 4-bromophenyl group, a 1-methylethyl group, and a 4,5-dihydrooxazoline ring. Additionally, it features two methyl groups attached to the oxazoline ring, contributing to its unique structural and potential functional properties. 2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE is likely to be utilized in organic synthesis or serve as a building block for the creation of more intricate molecular structures.
Uses
Used in Organic Synthesis:
2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE is used as a potential building block for the design of new drugs. Its structural features may contribute to the development of molecules with specific therapeutic targets, potentially leading to the creation of novel pharmaceutical agents.
Used in Chemical Research:
2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE is utilized in chemical research as a subject for studying the properties and reactivity of complex organic molecules. Understanding its behavior in various chemical reactions can provide insights into the development of new synthetic methods and the discovery of new compounds with unique properties.
The specific applications and properties of 2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE are dependent on its chemical and physical characteristics, which can be influenced by factors such as purity and synthesis method. Further research and development are necessary to fully explore its potential uses and optimize its synthesis for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 192775-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,7,7 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 192775-97:
(8*1)+(7*9)+(6*2)+(5*7)+(4*7)+(3*5)+(2*9)+(1*7)=186
186 % 10 = 6
So 192775-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18BrNO/c1-13(2)9-17-12(16-13)14(3,4)10-5-7-11(15)8-6-10/h5-8H,9H2,1-4H3
192775-97-6Relevant articles and documents
A new and competitive synthetic approach for an antihistamine agent, bilastine
Kommera, Rajashekar,Yerrabelly, Jayaprakash Rao,Kasireddy, Venkateshwarreddy,Ghojala, Venkat Reddy,Singavarapu, Adilakshmi,Rebelli, Pradeep
, p. 815 - 821 (2018/11/06)
Efforts towards the novel synthesis of second generation non-sedating antihistamine drug, Bilastine was described in this manuscript. This competitive synthetic approach involves the convergent synthesis of Bilastine via simple Friedel-Crafts acylation as an alternate for earlier reported Stille and Suzuki couplings. The selectivity in Friedel-Crafts acylation reaction with chloro acetyl chloride on different substituted arenes was studied and employed the best conditions for the synthesis of Bilastine. Further synthetic approach involves the deoxygenation of aryl ketone to corresponding alkane in single step and finally provides Bilastine with 39% of improved overall yields, utilizing simple and cost-effective reagents, suitable for kilogram scale synthesis.