192775-97-6 Usage
General Description
The chemical "2-[1-(4-bromophenyl)-1-methylethyl]-4,4-dimethyl-4,5-dihydrooxazoline" is a compound with a complex structure. It contains a 4-bromophenyl group, a 1-methylethyl group, and a 4,5-dihydrooxazoline ring. The compound also has two methyl groups attached to the oxazoline ring. This chemical may be used in organic synthesis or as a building block for more complex molecules. Its precise application and properties would depend on its specific chemical and physical characteristics, which can vary based on factors such as purity and synthesis method.
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.