431966
4-Formylphenylboronic acid
≥95.0%
Manufacturer: Sigma Aldrich
CAS Number: 87199-17-5
Synonym(S): 4-(Dihydroxyboryl)benzaldehyde, 4-Boronobenzaldehyde, 4-Formylbenzeneboronic acid, p-Formylbenzeneboronic acid, p-Formylphenylboronic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 431966-1-G | In Stock | ₹ 1,720.00 |
| 5 G | 431966-5-G | In Stock | ₹ 9,212.08 |
| 25 G | 431966-25-G | In Stock | ₹ 21,370.00 |
431966 - 1 G
In Stock
Quantity
1
Base Price: ₹ 1,720.00
GST (18%): ₹ 309.60
Total Price: ₹ 2,029.60
Quality Level
100
Assay
≥95.0%
mp
237-242 °C (lit.)
SMILES string
OB(O)c1ccc(C=O)cc1
InChI
1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
InChI key
VXWBQOJISHAKKM-UHFFFAOYSA-N
Related Products
Description
- Application: 4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions[1][2] and it can be used as a reagent for:Palladium-catalyzed Suzuki-Miyaura cross-coupling in water.[3] Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides.[4] Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.[5] Triethylamine-catalyzed three-component Hantzsch condensations.[6] Copper-catalyzed nitrations.[7] Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta.[8] Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides.[9] Palladium-catalyzed aerobic oxidative cross-coupling reactions.[10] The synthesis of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells.[11]The synthesis of a novel protein synthesis inhibitor active against Gram-positive bacteria.[12]The Suzuki aryl-aryl coupling of the upper rim of hexahomotrioxacalix[3]arene.[13]A rhodium-catalyzed cyclization, converting 1,5-enynes to cyclopentenes and spiro-cyclopentenes.
- Other Notes: Contains varying amounts of anhydride
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
Hazard Classifications
Skin Sens. 1
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 100
Assay: ≥95.0%
mp: 237-242 °C (lit.)
SMILES string: OB(O)c1ccc(C=O)cc1
InChI: 1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
InChI key: VXWBQOJISHAKKM-UHFFFAOYSA-N
Quality Level:
100
Assay:
≥95.0%
mp:
237-242 °C (lit.)
SMILES string:
OB(O)c1ccc(C=O)cc1
InChI:
1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
InChI key:
VXWBQOJISHAKKM-UHFFFAOYSA-N
Quality Level: 200
Assay: 98%
mp: 160-163 °C (lit.)
SMILES string: ClC1=CC(=O)C(Cl)=CC1=O
InChI: 1S/C6H2Cl2O2/c7-3-1-5(9)4(8)2-6(3)10/h1-2H
InChI key: LNXVNZRYYHFMEY-UHFFFAOYSA-N
Quality Level:
200
Assay:
98%
mp:
160-163 °C (lit.)
SMILES string:
ClC1=CC(=O)C(Cl)=CC1=O
InChI:
1S/C6H2Cl2O2/c7-3-1-5(9)4(8)2-6(3)10/h1-2H
InChI key:
LNXVNZRYYHFMEY-UHFFFAOYSA-N
Quality Level: 100
Assay: 95%
mp: __
SMILES string: OC(=O)COCc1ccccc1
InChI: 1S/C9H10O3/c10-9(11)7-12-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)
InChI key: GRZHHTYDZVRPIC-UHFFFAOYSA-N
Quality Level:
100
Assay:
95%
mp:
__
SMILES string:
OC(=O)COCc1ccccc1
InChI:
1S/C9H10O3/c10-9(11)7-12-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)
InChI key:
GRZHHTYDZVRPIC-UHFFFAOYSA-N
Quality Level: 100
Assay: ≥96.0% (HPLC)
mp: 143-146 °C (lit.)
SMILES string: Oc1ccc(\N=N\c2ccccc2)c(O)c1
InChI: 1S/C12H10N2O2/c15-10-6-7-11(12(16)8-10)14-13-9-4-2-1-3-5-9/h1-8,15-16H/b14-13+
InChI key: __
Quality Level:
100
Assay:
≥96.0% (HPLC)
mp:
143-146 °C (lit.)
SMILES string:
Oc1ccc(\N=N\c2ccccc2)c(O)c1
InChI:
1S/C12H10N2O2/c15-10-6-7-11(12(16)8-10)14-13-9-4-2-1-3-5-9/h1-8,15-16H/b14-13+
InChI key:
__