153451-34-4 Usage
Uses
Used in Organic Synthesis:
(S)-N-tritylbut-3-en-2-aMine is used as an intermediate in organic synthesis for its ability to participate in various chemical reactions. The trityl group's protective nature allows for selective functionalization of the molecule, making it a valuable component in the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-N-tritylbut-3-en-2-aMine is used as a building block for the synthesis of bioactive compounds. Its stability and reactivity contribute to the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
(S)-N-tritylbut-3-en-2-aMine is also utilized in chemical research to study the properties and reactivity of enamines and trityl-protected amines. This knowledge can be applied to the design and synthesis of novel compounds with specific chemical and biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 153451-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,5 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153451-34:
(8*1)+(7*5)+(6*3)+(5*4)+(4*5)+(3*1)+(2*3)+(1*4)=114
114 % 10 = 4
So 153451-34-4 is a valid CAS Registry Number.
153451-34-4Relevant academic research and scientific papers
Conversion of Aziridinemethanol Sulfonate Esters to Allylic Amines via Tellurium Chemistry
Pepito, Aurora S.,Dittmer, Donald C.
, p. 7920 - 7925 (2007/10/03)
Sulfonate esters of aziridinemethanols are converted to allylic amines by treatment with telluride ion obtained by reduction of elemental tellurium. In the course of the reaction, tellurium(0) is reformed and may be reused, thus removing the need to dispose of a key reagent. The telluride reaction yields optically active allylic amines from optically active aziridinemethanols. In contrast to many ring-openings of aziridines by nucleophiles, activation by an electron-withdrawing substituent on nitrogen is not necessary and is even detrimental.
