Product Name :
2-Nitrobenzaldehyde (CAS 552-89-6)

Synonym :

Application :
2-Nitrobenzaldehyde is a potential starting material for synthesis

CAS:
552-89-6

Purity:
≥95%

Molecular Weight:
151.12

Formula :
C7H5NO3

Physical state:
Solid

solubility :
Soluble in 95% ethanol (5%), methanol (100 mg/ml), water (0.23 mg/ml at 25° C), ether, and chloroform.

Shipping Condition :
Store at room temperature

Melting point:
42-44° C (lit.)

SMILES:
C1=CC=C(C(=C1)C=O)[N+](=O)[O-]

References:
:2-Nitrobenzaldehyde: a convenient UV-A and UV-B chemical actinometer for drug photostability testing. | Allen, JM., et al. 2000. J Pharm Biomed Anal. 24: 167-78. PMID: 11130196Hydrogen-bonded dimers in 2-nitrobenzaldehyde hydrazone and a three-dimensional hydrogen-bonded framework in 3-nitrobenzaldehyde hydrazone. | Glidewell, C., et al. 2004. Acta Crystallogr C. 60: o686-9. PMID: 15345857Effects of 4,5-dimethoxy groups on the time-resolved photoconversion of 2-nitrobenzyl alcohols and 2-nitrobenzaldehyde into nitroso derivatives. | Görner, H. 2005. Photochem Photobiol Sci. 4: 822-8. PMID: 16189558Improved gas chromatographic method for determination of daminozide by alkaline hydrolysis and 2-nitrobenzaldehyde derivatization and survey results of daminozide in agricultural products.2-Amino-4-bromo-3-fluorobenzoic acid Chemscene | Steinbrecher, K., et al. 1990. J Assoc Off Anal Chem. 73: 512-5. PMID: 2211471Synthesis, characterization and biological activity of transition metal complexes with Schiff bases derived from 2-nitrobenzaldehyde with glycine and methionine. | Singh, BK., et al. 2012. Spectrochim Acta A Mol Biomol Spectrosc. 94: 143-51. PMID: 22522296Cloning, expression, purification, and characterization of a novel single-chain variable fragment antibody against the 2-nitrobenzaldehyde derivative of a furaltadone metabolite in Escherichia coli. | Yang, W., et al. 2012. Protein Expr Purif. 84: 140-6. PMID: 22609338Coupled Ca2+/H+ transport by cytoplasmic buffers regulates local Ca2+ and H+ ion signaling. | Swietach, P., et al. 2013. Proc Natl Acad Sci U S A. 110: E2064-73. PMID: 23676270Synthesis and Antibacterial Evaluation of New Thione Substituted 1,2,4-Triazole Schiff Bases as Novel Antimicrobial Agents.212127-83-8 Chemscene | Akbari Dilmaghani, K.PMID:33511870 , et al. 2015. Iran J Pharm Res. 14: 693-9. PMID: 26330857Design, Synthesis and Antibacterial Evaluation of Some New 2-Phenyl-quinoline-4-carboxylic Acid Derivatives. | Wang, X., et al. 2016. Molecules. 21: 340. PMID: 26978336Partially oxidized iridium clusters within dendrimers: size-controlled synthesis and selective hydrogenation of 2-nitrobenzaldehyde. | Higaki, T., et al. 2016. Nanoscale. 8: 11371-4. PMID: 27193739Suppressing Effect of 2-Nitrobenzaldehyde on Singlet Oxygen Generation, Fatty Acid Photooxidation, and Dye-Sensitizer Degradation. | Hajimohammadi, M., et al. 2018. Antioxidants (Basel). 7: PMID: 30567321The interaction of a thiosemicarbazone derived from R – (+) – limonene with lipid membranes. | Marquezin, CA., et al. 2021. Chem Phys Lipids. 234: 105018. PMID: 33232725Synthesis of Computationally Designed 2,5(6)-Benzimidazole Derivatives via Pd-Catalyzed Reactions for Potential E. coli DNA Gyrase B Inhibition. | Aroso, RT., et al. 2021. Molecules. 26: PMID: 33801316