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27329-70-0

27329-70-0 Structure

27329-70-0 Structure
IdentificationMore
[Name]

2-Formylfuran-5-boronic acid
[CAS]

27329-70-0
[Synonyms]

2-FORMYLFURAN-5-BORONIC ACID
5-FORMYL-2-FURANBORONIC ACID
(5-FORMYL-2-FURANYL)BORONIC ACID
5-FORMYL-2-FURYLBORONIC ACID
5-FORMYLFURAN-2-BORONIC ACID
AKOS BRN-0038
CHEMBRDG-BB 3200975
FFBA
RARECHEM AH PB 0213
TIMTEC-BB SBB004171
5-Borono-2-furaldehyde
5-FORMYLFURAN-2-BORONIC ACID TECH
2-FORMYLFURAN-5-BORONIC ACID 95%
2-FORMLFURAN-5-BORONIC ACID
5-Formylfuran-2-boronicacid,97%
2-Formylfuran-5-boronic acid, tech., 90%
2-fomylfuran-5-boronic acid
2-FORMAYLFURAN-5-BORONIC ACID
5-FORMYL-THIOBORONICACID
5-Formyl-2-furanboronic Acid (contains varying amounts of Anhydride)
[EINECS(EC#)]

628-001-7
[Molecular Formula]

C5H5BO4
[MDL Number]

MFCD01114696
[Molecular Weight]

139.9
[MOL File]

27329-70-0.mol
Chemical PropertiesBack Directory
[Appearance]

white to light beige powder
[Melting point ]

136 °C (dec.) (lit.)
[Boiling point ]

379.3±52.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[storage temp. ]

0-6°C
[solubility ]

1.38g/l
[form ]

powder
[pka]

7.11±0.53(Predicted)
[color ]

brown
[Water Solubility ]

Insoluble in water.
[Sensitive ]

Air Sensitive
[Detection Methods]

HPLC
[BRN ]

1637050
[InChI]

InChI=1S/C5H5BO4/c7-3-4-1-2-5(10-4)6(8)9/h1-3,8-9H
[InChIKey]

JUWYQISLQJRRNT-UHFFFAOYSA-N
[SMILES]

B(C1=CC=C(C=O)O1)(O)O
[CAS DataBase Reference]

27329-70-0(CAS DataBase Reference)
[Storage Precautions]

Store under nitrogen;Light sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
[Hazard Codes ]

C,Xi
[Risk Statements ]

R34:Causes burns.
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 .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S37/39:Wear suitable gloves and eye/face protection .
S27:Take off immediately all contaminated clothing .
[RIDADR ]

UN 3261 8/PG 3
[WGK Germany ]

3
[Hazard Note ]

Irritant
[TSCA ]

No
[HazardClass ]

IRRITANT, KEEP COLD
[PackingGroup ]

[HS Code ]

29321900
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Skin Corr. 1B
Raw materials And Preparation ProductsBack Directory
[Raw materials]

n-Butyllithium-->Ammonium chloride-->Triethyl orthoformate-->Triisopropyl borate-->Furfural-->5-Bromo-2-furaldehyde-->2-(1,3-DIOXOLAN-2-YL)FURAN-->2-Furaldehyde diethyl acetal-->Tetrahydrofuran-->Ethylbenzene
[Preparation Products]

ETHYL 4-(5-FORMYL-2-FURYL)BENZOATE-->5-(4-CHLOROPHENYL)-2-FURALDEHYDE-->5-PHENYL-2-FURALDEHYDE-->5-(3-FLUORO-PHENYL)-FURAN-2-CARBALDEHYDE-->Benzoic acid,2-(5-formyl-2-furanyl)-, methyl ester
Hazard InformationBack Directory
[Chemical Properties]

beige to brown powder
[Uses]

suzuki reaction
[Synthesis]

2-Furaldehyde diethyl acetal

13529-27-6

2-Formylfuran-5-boronic acid

27329-70-0

Under nitrogen protection, 20.16 g (0.118 mol) of 2-(diethoxymethyl)furan, 33.4 g (0.177 mol) of triisopropyl borate, and 40 mL of anhydrous tetrahydrofuran (THF) were added to a dry 500 mL three-necked flask equipped with a mechanical stirrer, an internal thermometer, and a dosing funnel. The water content of the reaction mixture was determined by Karl-Fischer titration to ensure that it was less than 800 μg/mL. the reaction mixture was cooled to an internal temperature of -10 °C. The reaction mixture was then purified to a temperature of -10 °C. The water content of the reaction mixture was determined by titration. With the temperature maintained at -10 °C to 0 °C, 84 mL (25 wt%, 1.84 M THF solution containing heptane and ethylbenzene from Chemmetal, content determined by titration, 1.3 equivalents) of LDA solution was slowly added through the addition funnel over a period of 1 hour. Upon completion of addition, the reaction mixture was transferred via cannula to a pre-cooled aqueous hydrochloric acid solution (prepared by mixing 33 mL of concentrated hydrochloric acid and 55 mL of water). The reaction temperature was controlled not to exceed 30 °C. The resulting tan slurry of 5-formylfuran-2-boronic acid was cooled to 0°C and filtered. The filter cake was washed twice with 20 mL of cold water to obtain 17.6 g of wet filter cake. The wet filter cake was dried in a vacuum oven at 40 °C to give 12.41 g of an off-white product, 5-formylfuran-2-boronic acid, in a total yield of 75%. The amount of unreacted furfural in the crude product was determined to be less than 0.1% by analysis.

[References]

[1] Patent: EP1403271, 2004, A1. Location in patent: Page 3, 4
[2] Organic and Biomolecular Chemistry, 2003, vol. 1, # 9, p. 1447 - 1449
Spectrum DetailBack Directory
[Spectrum Detail]

2-Formylfuran-5-boronic acid(27329-70-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Formylfuran-5-boronic acid, tech., 90%(27329-70-0)
[Alfa Aesar]

5-Formylfuran-2-boronic acid, 97%(27329-70-0)
[Sigma Aldrich]

27329-70-0(sigmaaldrich)
[TCI AMERICA]

5-Formyl-2-furanboronic Acid  (contains varying amounts of Anhydride)(27329-70-0)
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