30691-46-4 Usage
Uses
Used in Pharmaceutical Industry:
1-acetyl-5-broMo-2,3-dihydro-1H-indole-7-sulfonyl chloride is used as a key intermediate in the development of potential drug candidates. Its unique structure and reactivity enable the synthesis of complex molecules and natural products with potential therapeutic applications.
Used in Organic Chemistry Research:
1-acetyl-5-broMo-2,3-dihydro-1H-indole-7-sulfonyl chloride is used as a research tool in organic chemistry. Its sulfonyl chloride group allows for the introduction of the sulfonyl moiety into various organic molecules, facilitating the synthesis of novel compounds and the exploration of new chemical reactions.
Used in Synthesis of Complex Molecules and Natural Products:
1-acetyl-5-broMo-2,3-dihydro-1H-indole-7-sulfonyl chloride is utilized in the synthesis of complex molecules and natural products. Its unique structure and reactivity make it a valuable building block for the creation of diverse chemical compounds with potential applications in medicine and research.
Check Digit Verification of cas no
The CAS Registry Mumber 30691-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,9 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30691-46:
(7*3)+(6*0)+(5*6)+(4*9)+(3*1)+(2*4)+(1*6)=104
104 % 10 = 4
So 30691-46-4 is a valid CAS Registry Number.
30691-46-4Relevant academic research and scientific papers
A convenient synthesis of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives
Dorogov, Mikhail V.,Filimonov, Sergey I.,Kobylinsky, Dmitry B.,Ivanovsky, Sergey A.,Korikov, Pavel V.,Soloviev, Mikhail Y.,Khahina, Maria Y.,Shalygina, Elena E.,Kravchenko, Dmitry V.,Ivachtchenko, Alexandre V.
, p. 2999 - 3004 (2007/10/03)
A large number of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives were prepared in good yields and excellent purity starting from the corresponding heterocyclic compounds. At first, chlorosulfonates were generated by reaction of initial heterocycles with various sulfonating and chlorinating agents followed by their conversion into sodium sulfinates. Treatment of sulfinates with acrylic acid smoothly afforded a series of sulfonylpropionates, which were used as convenient reagents for the preparation of a large number of the corresponding carboxamide derivatives.
