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512214

Sigma-Aldrich

1-Thianthrenylboronic acid

≥95%

Synonym(s):

Thianthrene-1-boronic acid

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About This Item

Empirical Formula (Hill Notation):
C12H9BO2S2
CAS Number:
Molecular Weight:
260.14
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

≥95%

mp

146-149 °C (lit.)

functional group

thioether

SMILES string

OB(O)c1cccc2Sc3ccccc3Sc12

InChI

1S/C12H9BO2S2/c14-13(15)8-4-3-7-11-12(8)17-10-6-2-1-5-9(10)16-11/h1-7,14-15H

InChI key

FZEWPLIHPXGNTB-UHFFFAOYSA-N

Application

Reactant for:
  • Pd2+ and Cu2+ catalyzed oxidative cross-couplings
  • Preparation of biologically and pharmacologically active molecules
  • Suzuki-Miyaura cross-coupling reactions

Other Notes

Contains varying amounts of anhydride

Storage Class Code

11 - Combustible Solids

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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Articles

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

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