1310384-28-1 Usage
Description
1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is a specialized organoboronic acid derivative with a unique bicyclic structure, featuring a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The 1-Boc (tert-butoxycarbonyl) protective group attached to the nitrogen atom reduces its reactivity, while the presence of two chlorine atoms and a boronic acid function, with a boron atom bonded to an oxygen atom, contributes to its versatile chemical properties. 1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is primarily used in research applications across various fields of organic and medicinal chemistry.
Uses
Used in Organic Chemistry Research:
1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of complex organic molecules, facilitating the development of new chemical entities with potential applications in various industries.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is employed as a key component in the design and synthesis of novel bioactive molecules. Its structural features and reactivity enable the development of potential drug candidates with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Chemical Synthesis:
1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is utilized as a reagent in various chemical reactions, including cross-coupling, Suzuki-Miyaura, and other transition metal-catalyzed processes. Its boronic acid functionality allows for the formation of new carbon-carbon and carbon-heteroatom bonds, enabling the synthesis of diverse molecular architectures with potential applications in materials science, pharmaceuticals, and agrochemicals.
Used in Drug Discovery:
1-Boc-5,6-Dichloro-1H-indole-2-boronic acid is employed as a starting material or a key intermediate in the drug discovery process. Its unique structural features and reactivity enable the generation of novel chemical entities with potential therapeutic applications, contributing to the development of new drugs for the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1310384-28-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,8 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1310384-28:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*8)+(3*4)+(2*2)+(1*8)=111
111 % 10 = 1
So 1310384-28-1 is a valid CAS Registry Number.
