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680532

Sigma-Aldrich

3-(N,N-Dimethylamino)phenylboronic acid

≥95%

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About This Item

Empirical Formula (Hill Notation):
C8H12BNO2
CAS Number:
178752-79-9
Molecular Weight:
165.00
MDL number:
MFCD01318996
UNSPSC Code:
12352103
PubChem Substance ID:
24885572
NACRES:
NA.22

Assay

≥95%

mp

178-190 °C

SMILES string

CN(C)c1cccc(c1)B(O)O

InChI

1S/C8H12BNO2/c1-10(2)8-5-3-4-7(6-8)9(11)12/h3-6,11-12H,1-2H3

InChI key

YZQQHZXHCXAJAV-UHFFFAOYSA-N

General description

May contain varying amounts of anhydride

Application

Reactant involved in synthesis of different protein effector including:
  • Modulators of survival motor neuron protein
  • Glucokinase activators
  • Aryl ethers for use as Bacillus anthracis enoyl-ACP reductase inhibitors

Reactant involved in synthesis of:
  • Thiourea-functionalized paracyclophanes
  • Low-background fluorescent imaging agents for nitric oxide

Reactant to undergo regioselective iodination and bromination

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

680532-1G:
680532-VAR:
680532-10G:
680532-BULK:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Gözde Murat Saltan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 188, 372-381 (2017-08-02)
In an approach to develop efficient organic optoelectronic devices to be used in light-driven systems, a series of three thiophene linked benzimidazole conjugates were synthesized and characterized. The combination of two thiophene rings to a benzimidazole core decorated with different

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