2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Basic Information

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CAS Number

374790-93-9

Molecular Formula

C10H15BO3

Molecular Weight

194.04 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Basic Physical Properties

Boiling Point

255℃/760mmHg

Refractive Index

1.473-1.475

SMILES

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B1(OC(C(O1)(C)C)(C)C)C2=CC=CO2

InChI

InChI=1S/C10H15BO3/c1-9(2)10(3,4)14-11(13-9)8-6-5-7-12-8/h5-7H,1-4H3

InChIKey

GWEWQKZABZXLJH-UHFFFAOYSA-N

LogP

1.5788

Topological Polar Surface Area

31.6 Å²

Hydrogen Bond Donor/Acceptor

0 / 3

Complexity

211

Synonyms & References

English

CS-W015756
Furan-2-Boronic Acid Pinacol Cyclic Ester
furan-2-boronic acid pinacol cyclic ester, AldrichCPR
2-(furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-Furanboronic acid pinacol ester
FURAN-2-BORONIC ACID, PINACOL ESTER
EN300-365465
FT-0626570
1,3,2-Dioxaborolane,2-(2-furanyl)-4,4,5,5-tetramethyl-
374790-93-9
MFCD02094008
Furan-2-boronic acid pinacol ester
A22716
2'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan
AKOS004115093
DS-13700
SY011756
DTXSID90463327
1,3,2-DIOXABOROLANE, 2-(2-FURANYL)-4,4,5,5-TETRAMETHYL-
GWEWQKZABZXLJH-UHFFFAOYSA-N
AB10875
AM20090602
Z1255403300
2-(2-Furanyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(2-furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
FURAN-2-YLBORONIC ACID PINACOL ESTER
SCHEMBL824193
2-FURYLBORONIC ACID PINACOLESTER~2-(2-FURYL)-4,4,5,5-TETRA
AKOS BRN-1103
2-Furylboronic acid pinacol ester~2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Furan-2-boronic acid pinacol cyclic ester

MDL Number

MFCD02094008

Customs Code

2934999090

FAQ

What are the physical and chemical properties of 2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9)?

2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9) has a crystalline form with a molecular weight of approximately 252.27 g/mol. It is slightly soluble in water but soluble in organic solvents like dichloromethane and methanol. The compound is known for its reactivity in organoboron coupling reactions, particularly in the presence of palladium catalysts.

How is 2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9) typically synthesized?

2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9) is typically synthesized through the reaction of 2-bromofurandione with tetramethyl-1,3,2-dioxaborolane, facilitated by a palladium catalyst in the presence of a base. The reaction provides good yield and selectivity.

What industries use 2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9)?

2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9) is used in the pharmaceutical industry for the synthesis of various bioactive compounds, as well as in the polymer industry for the development of functional materials with enhanced properties. It is also utilized in sensor technology and semiconductor manufacturing for specific chemical reactions.

What precautions should be taken when handling 2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9)?

When handling 2-(2-Furyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 374790-93-9), it is essential to use personal protective equipment (PPE) such as gloves and safety goggles. The substance should be stored in a well-ventilated area and handled in a fume hood to minimize inhalation risks. In case of a spill, the area should be cleaned immediately with the appropriate cleaning agents. Always consult the Safety Data Sheet (SDS) for detailed safety information.