Thiophene-2-Boronic Acid Pinacol Ester

Suppliers

Names

[ CAS No. ]:
193978-23-3

[ Name ]:
Thiophene-2-Boronic Acid Pinacol Ester

[Synonym ]:
Thiophene-2-boronic acid,pinacol ester
2-(thiophene-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-thienyl)-
4,4,5,5-Tetramethyl-2-(2-thienyl)-1,3,2-dioxaborolane
Thiophene-2-Boronic Acid Pinacol Ester
2-(thiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4,4,5,5-Tetramethyl-2-(thien-2-yl)-1,3,2-dioxaborolane
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
T5SJ B- BT5OBOTJ D1 D1 E1 E1
MFCD05663878
4,4,5,5-Tetramethyl-2-(thiophen-2-yl)-1,3,2-dioxaborolane
2-(4,4,5,5-tetramethyl-1,3,2,-dioxaborolan-2-yl)-thiophene
4,4,5,5-tetramethyl-2-(thiophene-2-yl)-1,3,2-dioxaborolane
2-thiophene boronic pinacol ester
2-Thiopheneboronic Acid Pinacol Ester

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
286.5±13.0 °C at 760 mmHg

[ Melting Point ]:
68-70°C

[ Molecular Formula ]:
C10H15BO2S

[ Molecular Weight ]:
210.101

[ Flash Point ]:
127.1±19.8 °C

[ Exact Mass ]:
210.088577

[ PSA ]:
46.70000

[ LogP ]:
2.04730

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.501

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
T

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

Precursor & DownStream

Precursor

  • Bromothiophene
  • Isopropoxyboronic acid pinacol ester
  • Thiophene(SIV)
  • Pinacol
  • Triisopropylborate
  • Bis(pinacolato)diboron
  • Pinacolborane
  • 2-Iodothiophene
  • Thienylboronic acid
  • 2-Chlorothiophene

DownStream

  • 2,2'-BITHIOPHENE-5-CARBOXALDEHYDE
  • methylthiol
  • alpha-Terthiophene
  • alpha-Quarterthiophene
  • 4,7-dithien-2-yl-2,1,3-benzothiadiazole
  • 6-thiophen-2-ylpyridine-3-carbonitrile

Articles

Quinacridone-based molecular donors for solution processed bulk-heterojunction organic solar cells.

ACS Appl. Mater. Interfaces 2 , 2679-2686, (2010)

New soluble quinacridone-based molecules have been developed as electron donor materials for solution-processed organic solar cells. By functionalizing the pristine pigment core of quinacridone with s...

Kim, J.; et al

J. Polym. Sci. A Polym. Chem. 49 , 369-380, (2011)

Park, J.-H; et al.

Organic Electrochemistry 11 , 820-830, (2010)


More Articles

Related Compounds

  • 5-Bromothiophene-2-boronic acid pinacol ester
  • 5-Cyanothiophene-2-boronic acid pinacol ester
  • 4-octylthiophene-2-boronic acid pinacol ester
  • 4-Bromothiophene-2-boronic acid pinacol ester
  • 5-Ethylthiophene-2-boronic acid pinacol ester
  • 5-Acetylthiophene-2-boronic acid pinacol ester
  • Ovaprim
  • 2-[2-(2-Hydroxyethoxy)ethoxy]ethyl 2-(2-hydroxyethoxy)ethyl 3,4,5,6-tetrabromobenzene-1,2-dicarboxylate
  • Diethylene glycol monodecyl ether sulfate ammonium salt
  • Ammonium 2-[2-(tetradecyloxy)ethoxy]ethyl sulfate
  • Karlotoxin-2
  • 3,5,7,7-Tetrachloro-2,2,3,4,4,5,6,6,7-nonafluoroheptanoic acid
  • 2-(Perfluorohexyl)ethanol dihydrogen phosphate bis(2-hydroxyethyl)amine
  • Phosphorodithioic acid, O,aO-abis(4-adodecylphenyl) S-a(1-aphenylethyl) ester
  • Sodium (9E)-17-carboxyheptadec-9-ene-1-sulfonate
  • 5-Methylheptyl 4-butyl-13-methyl-4-({2-[(5-methylheptyl)oxy]-2-oxoethyl}sulfanyl)-7-oxo-8-oxa-3,5-dithia-4-stannapentadecan-1-oate
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.