2-Nitrobenzaldehyde - CAS 552-89-6
Catalog: |
BB028989 |
Product Name: |
2-Nitrobenzaldehyde |
CAS: |
552-89-6 |
Synonyms: |
2-nitrobenzaldehyde |
IUPAC Name: | 2-nitrobenzaldehyde |
Description: | 2-Nitrobenzaldehyde (CAS# 552-89-6) is a benzaldhyde with a nitro group substituted in the ortho position. 2-Nitrobenzaldehyde is used in the preparation of dyes and colorants such as Indigo carmine. 2-Nitrobenzaldehyde gas been shown to be a useful photoremovable protecting group as well as in the preparation of more effective ones such as o-Nitrophenylethylene glycol. |
Molecular Weight: | 151.12 |
Molecular Formula: | C7H5NO3 |
Canonical SMILES: | C1=CC=C(C(=C1)C=O)[N+](=O)[O-] |
InChI: | InChI=1S/C7H5NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5H |
InChI Key: | CMWKITSNTDAEDT-UHFFFAOYSA-N |
Boiling Point: | 153 °C (23 torr) |
Melting Point: | 41-44 °C |
Purity: | 98 % |
Density: | 1.284 g/cm3 |
Appearance: | Yellow crystalline powder or needles |
Storage: | Store at RT. |
MDL: | MFCD00007132 |
LogP: | 1.93050 |
GHS Hazard Statement: | H302 (97%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113512072-A | Metal iridium (III) complex and preparation method and application thereof | 20210720 |
CN-113501905-A | Preparation method of photoresponse DNA hydrogel based on photoinduced proton transfer process | 20210715 |
CN-113333025-A | Catalyst for preparing all-trans beta-carotene and preparation method and application thereof | 20210628 |
CN-113354676-A | Cysteine fluorescent probe and preparation method and application thereof | 20210628 |
CN-113214178-A | 3-aryl substituted anthranilic anhydride derivative and preparation method thereof | 20210528 |
PMID | Publication Date | Title | Journal |
30926317 | 20190525 | Rabbit dehydrogenase/reductase SDR family member 11 (DHRS11): Its identity with acetohexamide reductase with broad substrate specificity and inhibitor sensitivity, different from human DHRS11 | Chemico-biological interactions |
22953862 | 20121201 | Direct detection of 3-amino-5-methylmorpholino-2-oxazolidinone (AMOZ) in food samples without derivatisation step by a sensitive and specific monoclonal antibody based ELISA | Food chemistry |
22019453 | 20121101 | Light-induced spatial control of pH-jump reaction at smart gel interface | Colloids and surfaces. B, Biointerfaces |
22974237 | 20121016 | Influenza virus-membrane fusion triggered by proton uncaging for single particle studies of fusion kinetics | Analytical chemistry |
22846796 | 20120901 | Design, synthesis, antimicrobial, anti-inflammatory and analgesic activity of novel isoxazolyl pyrimido[4,5-b]quinolines and isoxazolyl chromeno[2,3-d]pyrimidin-4-ones | European journal of medicinal chemistry |
Complexity: | 164 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 151.026943022 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 151.026943022 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 62.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.7 |
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