436836

2-Thienylboronic acid

≥95.0%

Manufacturer: Sigma Aldrich

CAS Number: 6165-68-0

Synonym(S): 2-Thienylboric acid, 2-Thienylboronic acid, Thien-5-ylboronic acid, Thiophene-2-boronic acid

Select a Size

Pack Size SKU Availability Price
1 G 436836-1-G In Stock ₹ 2,070.00
5 G 436836-5-G In Stock ₹ 5,060.00

436836 - 1 G

₹ 2,070.00

In Stock

Quantity

1

Base Price: ₹ 2,070.00

GST (18%): ₹ 372.60

Total Price: ₹ 2,442.60

Quality Level

200

Assay

≥95.0%

form

solid

mp

138-140 °C (lit.)

storage temp.

2-8°C

SMILES string

OB(O)c1cccs1

InChI

1S/C4H5BO2S/c6-5(7)4-2-1-3-8-4/h1-3,6-7H

InChI key

ARYHTUPFQTUBBG-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
T1772-5G
2-Thiopheneboronic Acid (contains varying amounts of Anhydride), TCI America™
TCI America ₹ 7,734.62
50-176-5698
Sigma Aldrich Fine Chemicals Biosciences 2-Thienylboronic acid >=95.0% | 6165-68-0 | MFCD00151850 | 1G
Sigma Aldrich Fine Chemicals Biosciences ₹ 5,852.30
50-011-2869
Matrix Scientific Thiophene-2-boronic acid, 6165-68-0, MFCD00151850, 5g
Matrix Scientific ₹ 2,558.24
50-211-0685
Strem, An Ascensus Company CAS 6165-68-0. 25g. 2-Thiopheneboronic acid min. 97%. MFCD00151850
Strem, An Ascensus Company ₹ 36,140.54
50-139-1884
Aobchem Thiophene-2-boronic acid, AOBCHEM USA 10295-100G. 6165-68-0. MFCD00151850
Aobchem ₹ 14,345.85
AR0036E1
Thiophene-2-boronic acid
Aaron Chemicals LLC ₹ 256.68 - ₹ 5,219.16

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Description

  • Application: Reagent used forPalladium-catalyzed Suzuki-Miyaura cross-couplings[1] Alkylation, boration, coupling reaction, Suzuki coupling, and halogenation of fluorenyl bromide[2] Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer[3] Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters[4] Ligand-free Suzuki, Sonogashira, and Heck cross-coupling reactions[5] Copper-catalyzed nitration reactions[6] Geometry relaxation-induced Large Stokes shift in red-emitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes[7] Reagent used in Preparation ofPhotophysical properties of oxygen-containing polycyclic aromatic triptycenes[8] Donor unit for donor-acceptor-type polymers via N-alkylation, Suzuki coupling, and bromination[9] Aminopyridine-based inhibitors of mitotic kinase Nek2 with potential antipoliferative effects in cancer tumors[10]
  • Other Notes: Contains varying amounts of anhydride

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Precautionary Statements

P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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OB(O)c1cccs1

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1S/C4H5BO2S/c6-5(7)4-2-1-3-8-4/h1-3,6-7H

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ARYHTUPFQTUBBG-UHFFFAOYSA-N

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QNMBSXGYAQZCTN-UHFFFAOYSA-N

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