675903
4-(Methanesulfonyl)phenylboronic acid
≥95.0%
Manufacturer: Sigma Aldrich
CAS Number: 149104-88-1
Synonym(S): 4-(Methanesulfonyl)benzeneboronic acid, 4-(Methylsulfonyl)phenylboronic acid, 4-Methansulfonylphenylboronic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 675903-1-G | In Stock | ₹ 4,102.68 |
675903 - 1 G
In Stock
Quantity
1
Base Price: ₹ 4,102.68
GST (18%): ₹ 738.482
Total Price: ₹ 4,841.162
Quality Level
100
Assay
≥95.0%
form
solid
mp
289-293 °C
SMILES string
CS(=O)(=O)c1ccc(cc1)B(O)O
InChI
1S/C7H9BO4S/c1-13(11,12)7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key
VDUKDQTYMWUSAC-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | 4-(Methylsulfonyl)phenylboronic Acid (contains varying amounts of Anhydride), TCI America™ | TCI America | ₹ 10,523.88 | |
 | Boronic acid, B-[4-(methylsulfonyl)phenyl]- | Aaron Chemicals LLC | ₹ 427.80 - ₹ 6,502.56 | |
 | 4-(Methylsulfonyl)phenylboronic acid | ChemScene | ₹ 1,711.20 - ₹ 29,261.52 | |
 | 149104-88-1 | 4-Methylsulfonylphenylboronic acid | A2B Chem | ₹ 427.80 - ₹ 21,390.00 |
Related Products
Description
- General description: Contains varying amounts of anhydride
- Application: 4-(Methanesulfonyl)phenylboronic acid may be used as reagent for:sequential Suzuki cross-coupling reactions[1] Copper-catalyzed oxidative trifluoromethylthiolation of aryl boronic acids[2] directed metalation and regioselective functionalization of 3-bromofuran and related heterocycles[3] Barton-Zard pyrrole cyclocondensations and Baeyer-Villiger oxidations[4] diplar cycloaddition and palladium-catalyzed cross-coupling processes[5]continuous flow Suzuki reactions for odanacatib intermediate synthesis[6]Reagent used in Preparation ofdiarylaminopyridines as potential anti-malarial agents[1] hydropyranopyrazine via chloropyrazinecarboxaldehyde and olefination[7] biaryl sulfone derivatives as antagonists of the histamine H3 receptor[8] novel kinase inhibitor scaffolds with potential antitumor effects[9][10] Hepatitis C virus inhibition activity of N-hydroxyisoquinoline di
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Compare Similar Items
Show Difference
Quality Level: 100
Assay: ≥95.0%
form: solid
mp: 289-293 °C
SMILES string: CS(=O)(=O)c1ccc(cc1)B(O)O
InChI: 1S/C7H9BO4S/c1-13(11,12)7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key: VDUKDQTYMWUSAC-UHFFFAOYSA-N
Quality Level:
100
Assay:
≥95.0%
form:
solid
mp:
289-293 °C
SMILES string:
CS(=O)(=O)c1ccc(cc1)B(O)O
InChI:
1S/C7H9BO4S/c1-13(11,12)7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key:
VDUKDQTYMWUSAC-UHFFFAOYSA-N
Quality Level: 100
Assay: ≥95%
form: solid
mp: 84-94 °C85-90 °C (lit.)
SMILES string: CC(C)(C)OC(=O)n1c(cc2ccccc12)B(O)O
InChI: 1S/C13H16BNO4/c1-13(2,3)19-12(16)15-10-7-5-4-6-9(10)8-11(15)14(17)18/h4-8,17-18H,1-3H3
InChI key: SVIBPSNFXYUOFT-UHFFFAOYSA-N
Quality Level:
100
Assay:
≥95%
form:
solid
mp:
84-94 °C85-90 °C (lit.)
SMILES string:
CC(C)(C)OC(=O)n1c(cc2ccccc12)B(O)O
InChI:
1S/C13H16BNO4/c1-13(2,3)19-12(16)15-10-7-5-4-6-9(10)8-11(15)14(17)18/h4-8,17-18H,1-3H3
InChI key:
SVIBPSNFXYUOFT-UHFFFAOYSA-N
Quality Level: 100
Assay: 96%
form: solid
mp: 168-172 °C
SMILES string: CC(C)c1cc(C(C)C)c(c(c1)C(C)C)-c2c(C)c(C)c(C)c(C)c2P(C(C)(C)C)C(C)(C)C
InChI: 1S/C33H53P/c1-19(2)26-17-27(20(3)4)30(28(18-26)21(5)6)29-24(9)22(7)23(8)25(10)31(29)34(32(11,12)13)33(14,15)16/h17-21H,1-16H3
InChI key: RCRYEYMHBHPZQD-UHFFFAOYSA-N
Quality Level:
100
Assay:
96%
form:
solid
mp:
168-172 °C
SMILES string:
CC(C)c1cc(C(C)C)c(c(c1)C(C)C)-c2c(C)c(C)c(C)c(C)c2P(C(C)(C)C)C(C)(C)C
InChI:
1S/C33H53P/c1-19(2)26-17-27(20(3)4)30(28(18-26)21(5)6)29-24(9)22(7)23(8)25(10)31(29)34(32(11,12)13)33(14,15)16/h17-21H,1-16H3
InChI key:
RCRYEYMHBHPZQD-UHFFFAOYSA-N
Quality Level: 200
Assay: ≥99.9%
form: liquid
mp: __
SMILES string: __
InChI: __
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Quality Level:
200
Assay:
≥99.9%
form:
liquid
mp:
__
SMILES string:
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InChI:
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InChI key:
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