281192-91-4 Usage
Uses
Used in Pharmaceutical Research and Development:
1-METHYL-3-BROMO-7-AZAINDOLE is used as a building block in organic synthesis for the creation of potential drug candidates. Its versatility as an intermediate allows for the development of various biologically active molecules, contributing to the advancement of novel drugs and therapeutic agents.
Used in Medicinal Chemistry:
1-METHYL-3-BROMO-7-AZAINDOLE is utilized as a versatile intermediate in medicinal chemistry, enabling the synthesis of a wide range of biologically active compounds. Its unique structure facilitates the exploration of new chemical entities with potential therapeutic applications, thereby enhancing the discovery of innovative treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 281192-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,1,9 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 281192-91:
(8*2)+(7*8)+(6*1)+(5*1)+(4*9)+(3*2)+(2*9)+(1*1)=144
144 % 10 = 4
So 281192-91-4 is a valid CAS Registry Number.
281192-91-4Relevant articles and documents
Selective methylation of NH-containing heterocycles and sulfonamides using n, N -dimethylformamide dimethylacetal based on calculated pKa Measurements
Fairley, Gary,Hall, Catherine,Greenwood, Ryan
, p. 570 - 574 (2013/04/10)
The use of N,N-dimethylformamide dimethylacetal (DMF-DMA) as a suitable methylating agent for the methylation of NH-containing groups and heterocycles has been investigated. Use of ReactArray and calculated pKa measurements have allowed additional helpful information to be collated to determine optimum reaction conditions for a variety of substrates.
A facile synthesis of 1-alkyl-7-azaisatins
Tatsugi, Jiro,Zhiwei, Tong,Amano, Tomohiro,Izawa, Yasuji
, p. 1145 - 1150 (2007/10/03)
1-Alkyl-7-azaisatins are synthesized from the reaction of 1-alkyl-7- azaindoles with bromine in dichloromethane and subsequent oxidation with N- bromosuccinimide - dimethyl sulfoxide reagent. 1-Alkyl-7-azaindoles are readily available in high yields from