All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C8H12BNO2
CAS Number:
Molecular Weight:
165.00
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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assay
≥95%
mp
178-190 °C
functional group
amine
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:
Reactant involved in synthesis of:
Reactant to undergo regioselective iodination and bromination
- 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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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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