3-Formylbenzoic acid

3-Formylbenzoic acid Structure
3-Formylbenzoic acid structure
Common Name 3-Formylbenzoic acid
CAS Number 619-21-6 Molecular Weight 150.131
Density 1.3±0.1 g/cm3 Boiling Point 331.7±25.0 °C at 760 mmHg
Molecular Formula C8H6O3 Melting Point 173-175 °C(lit.)
MSDS USA Flash Point 168.6±19.7 °C
Symbol GHS07
GHS07
Signal Word Warning

Novel styrylbenzene derivatives for detecting amyloid deposits.

Clin. Chim. Acta 436 , 27-34, (2014)

Various styrylbenzene compounds were synthesized and evaluated as mainly Aβ amyloid sensors. These compounds, however, cannot be used for detecting amyloid deposition in peripheral nerves because of the inherent sensitivity of the compounds. These compounds o...

Synthesis and evaluation of 3-(dihydroxyboryl)benzoic acids as D,D-carboxypeptidase R39 inhibitors.

J. Med. Chem. 52 , 6097-106, (2009)

Penicillin binding proteins (PBPs) catalyze steps in the biosynthesis of bacterial cell walls and are the targets for the beta-lactam antibiotics. Non-beta-lactam based antibiotics that target PBPs are of interest because bacteria have evolved resistance to t...

Synthesis of Alicyclic-lactams via the Ugi Reaction on a Solid Support. Gedey S, et al.

Lett. Org. Chem. 1(3) , 215-20, (2004)

Synthesis, binding properties and self-functionalization of a steroid-capped porphyrin. Richard P and Jeremy KM.

J. Chem. Soc. Chem. Commun. 8 , 574-77, (1991)

Synthesis of 4-amino-6-(hetero)arylalkylamino-1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives as potent A(2A) adenosine receptor antagonists.

Bioorg. Med. Chem. 11(24) , 5509-18, (2003)

In previous papers (Colotta, V. et al. Arch. Pharm. Pharm. Med. Chem. 1999, 332, 39. Colotta, V. et al. J. Med. Chem. 2000, 43, 1158) we reported the synthesis and binding affinity at bovine (b) A(1) and A(2A) and human (h) A(3) adenosine receptors (ARs) of t...

Impact of linker strain and flexibility in the design of a fragment-based inhibitor.

Nat. Chem. Biol. 5 , 407-13, (2009)

The linking together of molecular fragments that bind to adjacent sites on an enzyme can lead to high-affinity inhibitors. Ideally, this strategy would use linkers that do not perturb the optimal binding geometries of the fragments and do not have excessive c...