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1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid

Base Information
  • Chemical Name:1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid
  • CAS No.:877060-46-3
  • Molecular Formula:C13H11BN2O4S
  • Molecular Weight:302.118
  • Hs Code.:2933990090
  • Mol file:877060-46-3.mol
1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid

Synonyms:Boronicacid, [1-(phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridin-2-yl]- (9CI)

Suppliers and Price of 1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Chemenu
  • (1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridin-2-yl)boronicacid 95+%
  • 1g
  • $ 965.00
  • American Custom Chemicals Corporation
  • 1-(PHENYLSULFONYL)-1H-PYRROLO[3,2-C]PYRIDINE-2-YLBORONIC ACID 98.00%
  • 1G
  • $ 2130.45
  • American Custom Chemicals Corporation
  • 1-(PHENYLSULFONYL)-1H-PYRROLO[3,2-C]PYRIDINE-2-YLBORONIC ACID 98.00%
  • 5MG
  • $ 495.18
Total 3 raw suppliers
Chemical Property of 1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid
Chemical Property:
  • PSA:100.80000 
  • LogP:1.03390 
  • Storage Temp.:2-8°C 
Purity/Quality:

98%min *data from raw suppliers

(1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridin-2-yl)boronicacid 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid

There total 4 articles about 1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine-2-ylboronic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaH / tetrahydrofuran / 0.5 h / 20 °C
1.2: 84 percent / tetrahydrofuran / 20 °C
2.1: N,N,N',N'-tetramethylethylenediamine; LDA / tetrahydrofuran; heptane; ethylbenzene / 0.5 h / -20 °C
2.2: tetrahydrofuran; hexane; ethylbenzene / 5 h / -20 °C
3.1: 165 mg / aq. HCl
With hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene;
DOI:10.1055/s-2005-916028
Guidance literature:
Multi-step reaction with 2 steps
1.1: N,N,N',N'-tetramethylethylenediamine; LDA / tetrahydrofuran; heptane; ethylbenzene / 0.5 h / -20 °C
1.2: tetrahydrofuran; hexane; ethylbenzene / 5 h / -20 °C
2.1: 165 mg / aq. HCl
With hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene;
DOI:10.1055/s-2005-916028
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaH / tetrahydrofuran / 0.5 h / 20 °C
1.2: 84 percent / tetrahydrofuran / 20 °C
2.1: N,N,N',N'-tetramethylethylenediamine; LDA / tetrahydrofuran; heptane; ethylbenzene / 0.5 h / -20 °C
2.2: tetrahydrofuran; hexane; ethylbenzene / 5 h / -20 °C
3.1: 165 mg / aq. HCl
With hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene;
DOI:10.1055/s-2005-916028
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