268734-42-5 Usage
General Description
6-Phenylbenzo[d]isoxazol-3-amine is a chemical compound with the molecular formula C14H10N2O. It belongs to the class of organic compounds known as benzoisoxazoles, which are heterocyclic compounds containing a central isoxazole ring fused to a benzene ring. 6-Phenylbenzo[d]isoxazol-3-amine is used in pharmaceutical research and development as a building block for the synthesis of various biologically active compounds. It has potential applications in medicinal chemistry as a scaffold for the design of new drugs with therapeutic properties. Additionally, its unique structure and chemical properties make it a valuable molecule for studying reactions and mechanisms in organic chemistry. Overall, 6-Phenylbenzo[d]isoxazol-3-amine has significant potential in both pharmaceutical and academic research settings.
Check Digit Verification of cas no
The CAS Registry Mumber 268734-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,8,7,3 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 268734-42:
(8*2)+(7*6)+(6*8)+(5*7)+(4*3)+(3*4)+(2*4)+(1*2)=175
175 % 10 = 5
So 268734-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O/c14-13-11-7-6-10(8-12(11)16-15-13)9-4-2-1-3-5-9/h1-8H,(H2,14,15)
268734-42-5Relevant articles and documents
Application of a recyclable fluorous oxime in the convenient synthesis of 3-amino-1,2-benzisoxazoles and 4-amino-1H-2,3-benzoxazines
Ang, Wei Jie,Chu, Chi-Yuan,Chou, Tzyy-Chao,Lo, Lee-Chiang,Lam, Yulin
, p. 780 - 785 (2013/04/10)
A microwave-assisted, fluorous synthetic route to 3-amino-1,2- benzisoxazoles and 4-amino-1H-2,3-benzoxazines has been developed. The strategy comprises linking the respective 2-fluorobenzonitrile or 2-(bromomethyl) benzonitrile to a fluorous oxime tag to give an aryloxime intermediate which then undergoes cyclization with concomitant cleavage of the substrate-tag in acidic conditions to provide the desired product in good to moderate yields. In addition, the aryloxime intermediate could be subjected to further reactions to expand the compound library. The product could be easily separated using fluorous solid-phase extraction (F-SPE) and the fluorous ketone recovered could be converted back to the fluorous oxime and reused in the next run of the synthesis.
