794449-87-9 Usage
Structure
A derivative of benzisoxazole with a dimethylaminoethyl group and an ethoxy group attached to the benzisoxazole ring.
Biological activity
Potential biological activity due to its structure.
Pharmaceutical research
May be used as a building block for the synthesis of new compounds with therapeutic properties.
Organic synthesis
Can be used as a versatile intermediate for the creation of a variety of different molecules.
Handling and safety
Caution should be exercised when handling and using 1,2-Benzisoxazol-4-amine,3-ethoxy-4,5,6,7-tetrahydro-N,N-dimethyl-(9CI), as its specific hazards and risks are not specified.
Check Digit Verification of cas no
The CAS Registry Mumber 794449-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,4,4 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 794449-87:
(8*7)+(7*9)+(6*4)+(5*4)+(4*4)+(3*9)+(2*8)+(1*7)=229
229 % 10 = 9
So 794449-87-9 is a valid CAS Registry Number.
794449-87-9Relevant articles and documents
Selective inhibitors of glial GABA uptake: Synthesis, absolute stereochemistry, and pharmacology of the enantiomers of 3-hydroxy-4-amino-4,5,6,7-tetrahydro-1,2-benzisoxazole (exo-THPO) and analogues
Falch, Erik,Perregaard, Jens,Fr?lund, Bente,S?kilde, Birgitte,Buur, Anders,Hansen, Lene M.,Frydenvang, Karla,Brehm, Lotte,Bolvig, Tina,Larsson, Orla M.,Sanchez, Connie,White, Harold S.,Schousboe, Arne,Krogsgaard-Larsen, Povl
, p. 5402 - 5414 (2007/10/03)
3-Methoxy-4,5,6,7-tetrahydro-1,2-benzisoxazol-4-one (20a), or the corresponding 3-ethoxy analogue (20b), and 3-chloro- 4,5,6,7-tetrahydro-1,2-benzisothiazol-4-one (51) were synthesized by regioselective chromic acid oxidation of the respective bicyclic te
