594539

4-Methoxycarbonylphenylboronic acid

≥95%

Manufacturer: Sigma Aldrich

CAS Number: 99768-12-4

Synonym(S): (4-Carbomethoxyphenyl)boronic acid, 4-Carbomethoxybenzeneboronic acid, 4-Methoxycarbonylbenzeneboronic acid, 4-borono-benzoic acid 1-methyl ester, p-(Methoxycarbonyl)boronic acid, p-(Methoxycarbonyl)phenylboronic acid, p-borono-benzoic acid methyl ester, Methyl 4-boronobenzoate, Methyl p-boronobenzoate

Select a Size

Pack Size SKU Availability Price
1 G 594539-1-G In Stock ₹ 3,160.90
5 G 594539-5-G In Stock ₹ 9,850.75

594539 - 1 G

₹ 3,160.90

In Stock

Quantity

1

Base Price: ₹ 3,160.90

GST (18%): ₹ 568.962

Total Price: ₹ 3,729.862

Quality Level

100

Assay

≥95%

form

powder

mp

197-200 °C (lit.)

SMILES string

COC(=O)c1ccc(cc1)B(O)O

InChI

1S/C8H9BO4/c1-13-8(10)6-2-4-7(5-3-6)9(11)12/h2-5,11-12H,1H3

InChI key

PQCXFUXRTRESBD-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-139-1887
Aobchem 4-Methoxycarbonylphenylboronic acid, AOBCHEM USA 10265-100G. 99768-12-4. MFCD01632203
Aobchem ₹ 14,345.85
50-175-5318
Sigma Aldrich Fine Chemicals Biosciences 4-Methoxycarbonylphenylboronic acid >=95% | 99768-12-4 | MFCD01632203 | 1G
Sigma Aldrich Fine Chemicals Biosciences ₹ 5,587.07
50-175-5319
Sigma Aldrich Fine Chemicals Biosciences 4-Methoxycarbonylphenylboronic acid >=95% | 99768-12-4 | MFCD01632203 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 14,149.91
AR0035WD
Methyl 4-Boronobenzoate
Aaron Chemicals LLC ₹ 256.68 - ₹ 48,854.76
CS-W003977
Methyl 4-boronobenzoate
ChemScene ₹ 513.36 - ₹ 47,828.04
AB46513
99768-12-4 | 4-Methoxycarbonylphenylboronic acid
A2B Chem ₹ 342.24 - ₹ 1,197.84

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Description

  • Application: Reagent used forTandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence[1] Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides[2] One-pot ipso-nitration of arylboronic acids[3] Copper-catalyzed nitration[4] Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling[5] Reagent used in Preparation ofBiaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid[6]† Chromenones and their bradykinin B1 antagonistic activit[7]† Pt nanoparticles@Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injectio[8]† Salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor[9]†
  • Other Notes: Contains varying amount of anhydride

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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197-200 °C (lit.)

SMILES string:
COC(=O)c1ccc(cc1)B(O)O

InChI:
1S/C8H9BO4/c1-13-8(10)6-2-4-7(5-3-6)9(11)12/h2-5,11-12H,1H3

InChI key:
PQCXFUXRTRESBD-UHFFFAOYSA-N

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InChI:
1S/C8H7BrO3/c9-4-8(12)6-2-1-5(10)3-7(6)11/h1-3,10-11H,4H2

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RAULLGKGLGXMOM-UHFFFAOYSA-N

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1S/C.Hf/q-1;+1

InChI key:
NVDNLVYQHRUYJA-UHFFFAOYSA-N