150691-04-6

Basic information

• Product Name: 2-(tert-Butylamino)sulfonylphenylboronic acid
• Synonyms: AKOS BRN-0531;2-(T-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID;(2-((TERT-BUTYLAMINO)SULFANYL)PHENYL) BORONIC ACID;2-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID;CHEMBRDG-BB 3200963;{2-[(tert-butylamino)sulfonyl]phenyl}boronic acid(SALTDATA: FREE);(2-(N-(tert-Butyl)sulfamoyl)phenyl)boronic acid;N-TERT-BUTYLBENZENESULFONAMIDE-2-BORONIC ACID
• CAS NO: 150691-04-6
• Molecular Formula: C₁₀H₁₆BNO₄S
• Molecular Weight: 257.11
• Product Categories: Aryl;Organoborons;Sulfonamide
• Mol File: 150691-04-6.mol
• Article Data: 20

Chemical Properties

• Melting Point: 118-119 °C
• Boiling Point: 443.205 °C at 760 mmHg
• Flash Point: 221.843 °C
• Appearance: /
• Density: 1.283 g/cm³
• Vapor Pressure: 1.23E-08mmHg at 25°C
• Refractive Index: 1.554
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.00±0.53(Predicted)
• CAS DataBase Reference: 2-(tert-Butylamino)sulfonylphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(tert-Butylamino)sulfonylphenylboronic acid(150691-04-6)
• EPA Substance Registry System: 2-(tert-Butylamino)sulfonylphenylboronic acid(150691-04-6)

Safety Data

• Hazardous Substances Data: 150691-04-6(Hazardous Substances Data)

Usage

Description

2-(tert-Butylamino)sulfonylphenylboronic acid is a boronic acid derivative with the molecular formula C10H16BNO4S. It features a boron atom attached to a phenyl ring and a sulfonamide group, with a tert-butylamino group providing steric hindrance at the boron center. 2-(tert-Butylamino)sulfonylphenylboronic acid is known for its reactivity and stability in organic synthesis, particularly in forming carbon-carbon and carbon-heteroatom bonds.

Uses

Used in Organic Synthesis:
2-(tert-Butylamino)sulfonylphenylboronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure and reactivity make it a valuable component in creating complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-(tert-Butylamino)sulfonylphenylboronic acid is used as a building block or intermediate in the synthesis of various drug candidates. Its potential applications include the development of new therapeutic agents and the improvement of existing medications.
Used as a Ligand in Catalytic Reactions:
2-(tert-Butylamino)sulfonylphenylboronic acid is utilized as a ligand in catalytic reactions, enhancing the efficiency and selectivity of various chemical transformations. Its presence can improve the performance of catalysts and facilitate specific reaction pathways.
Used in Optoelectronic Materials Development:
In the optoelectronics industry, 2-(tert-Butylamino)sulfonylphenylboronic acid is used in the development of materials for optoelectronic devices. Its properties contribute to the creation of advanced materials with improved performance in areas such as solar cells, light-emitting diodes, and photodetectors.

InChI:InChI=1/C10H16BNO4S/c1-10(2,3)12-17(15,16)9-7-5-4-6-8(9)11(13)14/h4-7,12-14H,1-3H3

Upstream product

• 98-09-9 benzenesulfonyl chloride 
• 121-43-7 Trimethyl borate 
• 2512-24-5 N-tert-butylbenzenesulfonamide 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 203512-83-8 2-Amino-5-(2-t-butylaminosulfonyl-phenyl)-pyridine 
• 1026901-65-4 2-(5-amino-pyridin-2-yl)-N-tert-butyl-benzenesulfonamide 
• 316364-80-4 1N-(4'-(o-tert-butylaminosulfonylphenyl)phenylcarbonyl)methyl-6-cyanobenzimidazole 
• 477717-00-3 methyl 4-(2'-tert-butylaminosulfonyl)phenyl-2-methyl benzoate 
• 476352-82-6 3-{2-[5-(2'-tert-butylaminosulfonyl)phenyl-1-oxoisoindolin-2-yl]ethoxy}benzonitrile 
• 330802-69-2 2-(6-methoxy-naphthalen-2-yl)-5-methyl-2H-pyrazole-3-carboxylic acid (2'-sulfamoyl-biphenyl-4-yl)-amide 
• 330803-42-4 5-methyl-2-naphthalen-2-yl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide 
• 330802-25-0 2-(3-cyano-naphthalen-2-yl)-5-methyl-2H-pyrazole-3-carboxylic acid (2'-sulfamoyl-biphenyl-4-yl)-amide 
• 330803-82-2 2-(6-bromo-naphthalen-2-yl)-5-methyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide 

Relevant articles and documents

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