55809-36-4 Usage
Description
3-Amino-5-tert-butylisoxazole is an organic compound that is characterized by the presence of an isoxazole ring with a tert-butyl group and an amino group attached to it. It is a versatile molecule with potential applications in various fields due to its unique structure and reactivity.
Uses
Used in Pharmaceutical Industry:
3-Amino-5-tert-butylisoxazole is used as a catalyst in the amination of aryl bromides, a crucial reaction in the synthesis of various pharmaceutical compounds. The amination process is catalyzed by Pd(dba)3 and Xantphos, which facilitate the formation of amines from aryl bromides, leading to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3-Amino-5-tert-butylisoxazole is also identified as a degradation product of the herbicide isouron. In this context, it plays a role in the environmental fate and breakdown of the herbicide, which is essential for understanding its impact on the ecosystem and agricultural practices. The study of such degradation products helps in the development of safer and more environmentally friendly herbicides.
Check Digit Verification of cas no
The CAS Registry Mumber 55809-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55809-36:
(7*5)+(6*5)+(5*8)+(4*0)+(3*9)+(2*3)+(1*6)=144
144 % 10 = 4
So 55809-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O/c1-7(2,3)5-4-6(8)9-10-5/h4H,1-3H3,(H2,8,9)
55809-36-4Relevant articles and documents
Preparation method 3 -amino -5 -alkyl isoxazole
-
Paragraph 0034-0035; 0038; 0039-0040; 0043, (2020/06/05)
The invention discloses a preparation method of 3-amino-5-alkyl isoxazole, realizes preparation through two steps and belongs to the technical field of organic chemistry. By starting from easily obtained aldehyde, after the addition with acetonitrile under the existence of metal alkali, an intermediate of hydroxy nitrile is obtained; then, the hydroxy nitrile reacts with hydroxylamine; ring closing reaction is performed under the existence of Lewis acid; after autoxidation, the 3-amino-5-alkyl isoxazole is obtained. The raw materials in the reaction process are very commons; chloroform or tetrachloromethane in a traditional method is avoided; potential industrial amplification prospects are realized.
THIENO[3,2-D]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASES
-
Paragraph 0288; 0289; 0290, (2015/01/06)
Provided are a thieno[3,2-d]pyrimidine derivative of formula (I) or a pharmaceutically acceptable salt thereof having inhibitory activity for protein kinase, and a pharmaceutical composition comprising same for prevention and treatment of abnormal cell growth diseases.
THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASES
-
Page/Page column 42; 43, (2013/07/19)
Provided are a thieno[3,2-d]pyrimidine derivative of formula (I) or a pharmaceutically acceptable salt thereof having inhibitory activity for protein kinase, and a pharmaceutical composition comprising same for prevention and treatment of abnormal cell growth diseases
