436095-50-0 Usage
Description
2-amino-N-propylbenzenesulfonamide is an organic compound with the molecular formula C9H14N2SO2. It is a white crystalline solid that is soluble in water and has a role as a research reagent. 2-amino-N-propylbenzenesulfonamide is characterized by its amino and sulfonamide functional groups, which contribute to its reactivity and potential applications in various fields.
Uses
Used in Pharmaceutical Research:
2-amino-N-propylbenzenesulfonamide is used as a research reagent for the preparation of pyrimidine derivatives. These derivatives have numerous pharmaceutical applications, making this compound a valuable tool in the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic chemistry, 2-amino-N-propylbenzenesulfonamide can be utilized as a building block or intermediate in the synthesis of more complex molecules. Its unique functional groups allow for a variety of reactions, making it a versatile compound for creating novel chemical entities with potential applications in various industries.
Used in Chemical Research:
As a research reagent, 2-amino-N-propylbenzenesulfonamide is also employed in chemical research to study the properties and reactivity of amino and sulfonamide groups. This can lead to a better understanding of the underlying chemistry and the development of new synthetic methods or applications for related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 436095-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,0,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 436095-50:
(8*4)+(7*3)+(6*6)+(5*0)+(4*9)+(3*5)+(2*5)+(1*0)=150
150 % 10 = 0
So 436095-50-0 is a valid CAS Registry Number.
436095-50-0Relevant articles and documents
One-pot synthesis ofN-substituted benzannulated triazolesviastable arene diazonium salts
Faggyas, Réka J.,McGrory, Rochelle,Sutherland, Andrew
, p. 6127 - 6140 (2021/07/21)
A mild and effective one-pot synthesis of 1,2,3-benzotriazin-4(3H)-ones and benzothiatriazine-1,1(2H)-dioxide analogues has been developed. The method involves the diazotisation and subsequent cyclisation of 2-aminobenzamides and 2-aminobenzenesulfonamidesviastable diazonium salts, prepared using a polymer-supported nitrite reagent andp-tosic acid. The transformation was compatible with a wide range of aryl functional groups and amide/sulfonamide-substituents and was used for the synthesis of pharmaceutically important targets. The synthetic utility of the one-pot diazotisaton-cyclisation process was further demonstrated with the preparation of an α-amino acid containing 1,2,3-benzotriazin-4(3H)-one.
