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Phenethylboronic acid

CAS No.
34420-17-2
Chemical Name:
Phenethylboronic acid
Synonyms
2-PHENYLETHYL-1-BORONIC ACID;RARECHEM AH PB 0199;Phenethylboronic aci;PHENETHYLBORONIC ACID;Phenethylboranic acid;Phenylethylboronic acid;B-Phenethylboronic acid;2-Phenylethylboronicaci;PHENYLETHANEBORONIC ACID;2-PHENYLETHYLBORONIC ACID
CBNumber:
CB5258024
Molecular Formula:
C8H11BO2
Molecular Weight:
149.98
MDL Number:
MFCD01631226
MOL File:
34420-17-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:11:03

Phenethylboronic acid Properties

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
CAS DataBase Reference 34420-17-2(CAS DataBase Reference)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HazardClass  IRRITANT
HS Code  2931900090
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

Phenethylboronic acid price More Price(47)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 588423 Phenethylboronic acid 34420-17-2 1g $69.6 2026-04-30 Buy
Sigma-Aldrich 588423 Phenethylboronic acid 34420-17-2 10g $293 2026-04-30 Buy
TCI Chemical P2476 2-Phenylethylboronic Acid (contains varying amounts of Anhydride) 34420-17-2 1g $28 2026-04-30 Buy
TCI Chemical P2476 2-Phenylethylboronic Acid (contains varying amounts of Anhydride) 34420-17-2 5g $109 2026-04-30 Buy
Activate Scientific AS50959 2-Phenyl-1-ethylboronic acid 98% 34420-17-2 5g $31 2026-06-04 Buy
Product number Packaging Price Buy
588423 1g $69.6 Buy
588423 10g $293 Buy
P2476 1g $28 Buy
P2476 5g $109 Buy
AS50959 5g $31 Buy

Phenethylboronic acid Chemical Properties,Uses,Production

Chemical Properties

off-white powder

Uses

Phenethylboronic acid is a good inhibitor of chymotrypsin.

Uses

2-Phenylethylboronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions, reactions with α-diazocarbonyl compounds, C-H functionalization of quinones, cross-coupling with aromatic amines and arylation & alkylation of diphenylisoxazole. It has been also used as reactant in studies of the stability of boronic esters to hydrolysis.

Uses

Reactant involved in:• ;Suzuki-Miyaura cross-coupling reactions1• ;Reactions with α-diazocarbonyl compounds2• ;C-H functionalization of quinones3• ;Cross-coupling with aromatic amines4• ;Arylation and alkylation of diphenylisoxazole5Reactant used in studies of the stability of boronic esters to hydrolysis6

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

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View Lastest Price from Phenethylboronic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
 Phenethylboronic acid pictures 2019-07-06 Phenethylboronic acid
34420-17-2
$8.00 1kg 99% 10MT Career Henan Chemical Co

Phenethylboronic acid Spectrum

2-PHENYL-1-ETHYLBORONIC ACID 2-PHENYLETHANEBORONIC ACID 2-PHENYLETHYLBORONIC ACID RARECHEM AH PB 0199 PHENYLETHANEBORONIC ACID PHENETHYLBORONIC ACID Phenylethylboronic acid Phenylethaneboronic acid, 2-Phenylethyl-1-boronic acid B-Phenethylboronic acid Phenethylboranic acid Phenethylboronic acid ,97% Phenethylboronic aci 2-Phenylethylboronic Acid (contains varying amounts of Anhydride) Phenethylboronic acid(Contains varying amounts of anhydride) Boronic acid, B-(2-phenylethyl)- 2-Phenylethylboronicaci 2-Phenyl-1-ethylboronic acid - [P4926] 2-PHENYLETHYL-1-BORONIC ACID 34420-17-2 C6H5CH2CH2BOH2 Organometallic Reagents Boronic Acids and Derivatives Boronic Acids Alkyl Alkyl Boronic Acids Boronic Acids and Derivatives Chemical Synthesis Organometallic Reagents OLED materials,pharm chemical,electronic Boronic Acids Boronic Acids and Derivatives Aryl Boronic acid Organoborons Alkyl blocks BoronicAcids Boronic acids