| Identification | More | [Name]
4-Ethoxycarbonylphenylboronic acid | [CAS]
4334-88-7 | [Synonyms]
4-CARBETHOXY-PHENYL-BORONIC ACID
4-(ETHOXYCARBONYL)BENZENEBORONIC ACID
4-ETHOXYCARBONYLPHENYLBORONIC ACID
AKOS BRN-0420
ETHYL 4-BORONOBENZOATE
P-ETHOXYCARBONYLPHENYLBORONIC ACID
Ethyl 4-Boronobenzoat
4-Borono-benzoic Acid 1-Ethyl Ester
4-Carboethoxybenzeneboronic Acid
p-Borono-benzoic Acid 1-Ethyl Ester
4-(Ethoxycarbonyl)Phenylboroni
4-ETHOXYCARBONYLPHENYLBORONIC ACID 98% | [EINECS(EC#)]
206-141-6 | [Molecular Formula]
C9H11BO4 | [MDL Number]
MFCD02179441 | [Molecular Weight]
193.99 | [MOL File]
4334-88-7.mol |
| Chemical Properties | Back Directory | [Appearance]
white to off-white powder | [Melting point ]
135 °C (dec.) (lit.) | [Boiling point ]
355.5±44.0 °C(Predicted) | [density ]
1.21±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
Powder | [pka]
7.69±0.10(Predicted) | [color ]
White to off-white | [InChIKey]
ZLNFACCFYUFTLD-UHFFFAOYSA-N | [CAS DataBase Reference]
4334-88-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,T | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R26:Very Toxic by inhalation.
R22:Harmful if swallowed. | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37:Wear suitable protective clothing and gloves .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) . | [WGK Germany ]
3 | [Hazard Note ]
Irritant | [TSCA ]
No | [HazardClass ]
IRRITANT | [HS Code ]
29163990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to off-white powder | [Uses]
Reactant involved in:• ;Oxidative hydroxylation for the preparation of phenols1• ;Homolytic aromatic substitution2• ;Cross-coupling with α-bromocarbonyl compounds3• ;Suzuki-coupling reaction with quinoline carboxylates4• ;Trifluoromethylation5• ;Carbometalation of ynamides6 | [Uses]
suzuki reaction |
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