ChemicalBook--->CAS DataBase List--->34420-17-2

34420-17-2

34420-17-2 Structure

34420-17-2 Structure
IdentificationMore
[Name]

Phenethylboronic acid
[CAS]

34420-17-2
[Synonyms]

2-PHENYL-1-ETHYLBORONIC ACID
2-PHENYLETHANEBORONIC ACID
2-PHENYLETHYL-1-BORONIC ACID
2-PHENYLETHYLBORONIC ACID
PHENETHYLBORONIC ACID
PHENYLETHANEBORONIC ACID
RARECHEM AH PB 0199
Phenylethylboronic acid
Phenylethaneboronic acid, 2-Phenylethyl-1-boronic acid
B-Phenethylboronic acid
Phenethylboranic acid
[Molecular Formula]

C8H11BO2
[MDL Number]

MFCD01631226
[Molecular Weight]

149.98
[MOL File]

34420-17-2.mol
Chemical PropertiesBack Directory
[Melting point ]

76-81 °C (lit.)
[Boiling point ]

310.4±35.0 °C(Predicted)
[density ]

1.077±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

powder to crystal
[pka]

10.12±0.43(Predicted)
[color ]

White to Almost white
[InChI]

InChI=1S/C8H11BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5,10-11H,6-7H2
[InChIKey]

VPRUMANMDWQMNF-UHFFFAOYSA-N
[SMILES]

B(CCC1=CC=CC=C1)(O)O
[Uses]

Phenethylboronic acid is a good inhibitor of chymotrypsin.
[CAS DataBase Reference]

34420-17-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2931900090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

1,2-Ethanediyl, 1-phenyl- (9CI)

292638-84-7

Phenethylboronic acid

34420-17-2

A solution was prepared by dissolving styrene (2.083 g, 20 mmol) and trimethylsilane (1.484 g, 20 mmol) in hexane (6 mL) at -80 °C. The solution was slowly added dropwise to a solution of BBr3 (5.010 g, 20 mmol) in hexane (6 mL). The reaction system was controlled to gradually warm up to room temperature over a period of 2 hours. Upon completion of the reaction, the solvent was removed by evaporation under vacuum. Water (4 mL) was added to the residue, at which point the release of gaseous HBr and an increase in the temperature of the system was observed. After cooling the system to room temperature, the solvent was again evaporated under vacuum. The resulting white precipitate was purified by recrystallization from a minimal amount of water to give 2.73 g (69% yield) of 2-phenylethylboronic acid. Methanol (0.81 mL, 20 mmol) was added to a suspension of 2-phenylethylboronic acid (1.5 g, 10 mmol) in pentane (6 mL) and the reaction was stirred for 20 min at room temperature. MgSO4 was then added and stirring was continued for 10 minutes before the organic phase was separated. Methanol (0.81 mL, 20 mmol) was added again to the aqueous phase and stirred at room temperature for 20 min before adding MgSO4 and stirring for 10 min to separate the organic phase. All organic phase extracts were combined, concentrated and the residue was purified by vacuum distillation to give 1.19 g (67% yield) of a colorless liquid dimethyl 2-phenylborate.

[References]

[1] Tetrahedron Letters, 2003, vol. 44, # 42, p. 7789 - 7792
[2] Tetrahedron Letters, 2011, vol. 52, # 41, p. 5259 - 5263
[3] Journal of Organic Chemistry, 2008, vol. 73, # 5, p. 1898 - 1905
[4] Patent: WO2008/103016, 2008, A1. Location in patent: Page/Page column 7
Spectrum DetailBack Directory
[Spectrum Detail]

Phenethylboronic acid(34420-17-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

34420-17-2(sigmaaldrich)
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