1075-34-9 Usage
Description
5-Bromo-2-methylindole, a bromoalkylindole derivative, is a chemical compound that has been synthesized through the bromination of 2-methylindole. It is characterized by its distinct chemical structure, which can be identified through 1H NMR (nuclear magnetic resonance) spectroscopy. 5-BROMO-2-METHYLINDOLE holds potential for various applications across different industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
5-Bromo-2-methylindole is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting neurological and psychiatric disorders.
Used in Chemical Research:
In the field of chemical research, 5-Bromo-2-methylindole serves as a valuable compound for studying the properties and reactivity of bromoalkylindole derivatives. It can be used to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
5-Bromo-2-methylindole can be utilized as a building block for the development of novel materials with specific properties, such as optoelectronic materials or advanced polymers. Its unique structure may contribute to the creation of materials with enhanced performance characteristics.
Used in Analytical Chemistry:
As a compound with distinct spectroscopic features, 5-Bromo-2-methylindole can be employed as a reference material or standard in analytical chemistry. It can be used to calibrate instruments, validate analytical methods, or as an internal standard in quantitative analyses.
Used in Environmental Science:
5-Bromo-2-methylindole may also find applications in environmental science, particularly in the development of new methods for the detection and monitoring of pollutants or contaminants. Its unique chemical properties could be harnessed to create sensitive and selective sensors for environmental monitoring.
Check Digit Verification of cas no
The CAS Registry Mumber 1075-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1075-34:
(6*1)+(5*0)+(4*7)+(3*5)+(2*3)+(1*4)=59
59 % 10 = 9
So 1075-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrN/c1-6-4-7-5-8(10)2-3-9(7)11-6/h2-5,11H,1H3
1075-34-9Relevant articles and documents
Cu-Catalyzed Oxidation of C2 and C3 Alkyl-Substituted Indole via Acyl Nitroso Reagents
Zhang, Jun,Torabi Kohlbouni, Saeedeh,Borhan, Babak
supporting information, p. 14 - 17 (2019/01/08)
The selective oxidation of C2-alkyl-substituted indoles to 3-oxindole and the selective C-H oxygenation or amination of C2,C3-dialkyl-substituted indoles at C2 are reported under mild conditions. The position of the alkyl substitution on the indole directs the reaction to different pathways under similar conditions.
Asymmetric Hydrogenation of Unprotected Indoles Catalyzed by η6-Arene/N-Me-sulfonyldiamine-Ru(II) Complexes
Touge, Taichiro,Arai, Takayoshi
supporting information, p. 11299 - 11305 (2016/10/12)
Protecting-group-free transformation is a challenging and important issue in atom-economical organic synthesis. The η6-arene/N-Me-sulfonyldiamine-Ru(II)-BF4 complex-catalyzed asymmetric hydrogenation of 2-substituted unprotected indoles in weakly acidic hexafluoroisopropanol gives optically active indoline compounds with up to >99% ee. Under mild reaction media, halogen atoms and synthetically important protecting groups (e.g., silyl ether, acetal, benzyl ether, and ester) on indoles are maintained, which is advantageous for the synthesis of further complex indoline molecules.
HETEROCYCLIC COMPOUNDS FOR THE INHIBITION OF PASK
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Page/Page column 161, (2012/09/21)
Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
