4-Iodobenzaldehyde - CAS 15164-44-0
Catalog: |
BB010698 |
Product Name: |
4-Iodobenzaldehyde |
CAS: |
15164-44-0 |
Synonyms: |
4-iodobenzaldehyde |
IUPAC Name: | 4-iodobenzaldehyde |
Description: | 4-Iodobenzaldehyde (CAS# 15164-44-0) is a halogenated Benzaldehyde (B119740) which is mainly used as a precursor to other organic compounds, such as pharmaceuticals, and plastic additives. |
Molecular Weight: | 232.02 |
Molecular Formula: | C7H5IO |
Canonical SMILES: | C1=CC(=CC=C1C=O)I |
InChI: | InChI=1S/C7H5IO/c8-7-3-1-6(5-9)2-4-7/h1-5H |
InChI Key: | NIEBHDXUIJSHSL-UHFFFAOYSA-N |
Boiling Point: | 264.8 °C at 760 mmHg |
Melting Point: | 78-82 °C |
Purity: | 95 % |
Density: | 1.883 g/cm3 |
Appearance: | Yellow crystals |
Storage: | Keep Cold |
MDL: | MFCD00039576 |
LogP: | 2.10370 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113416138-A | Henry type reaction method of iron mediated aldehyde and bromonitromethane and product | 20210721 |
CN-113372186-A | Method for synthesizing biaryl compound | 20210617 |
CN-113321625-A | Synthetic method for preparing benzoxazole compound from catechol compound, ammonium acetate and aldehyde compound | 20210606 |
CN-113321627-A | Tafamidis derivative and synthetic method thereof | 20210606 |
CN-113121470-A | Preparation method of benzothiadiazine-1, 1-dioxide compound | 20210305 |
PMID | Publication Date | Title | Journal |
22763695 | 20120701 | Competing intermolecular interactions in some 'bridge-flipped' isomeric phenylhydrazones | Acta crystallographica. Section C, Crystal structure communications |
19019238 | 20081119 | Gamma probes and their use in tumor detection in colorectal cancer | International seminars in surgical oncology : ISSO |
14712036 | 20040101 | Hydrogen-bonded chains of rings in 3-iodobenzaldehyde 2,4-dinitrophenylhydrazone and 4-iodobenzaldehyde 2,4-dinitrophenylhydrazone, and a three-dimensional framework in 4-iodobenzaldehyde 4-nitrophenylhydrazone generated by the combination of N-H...O and C-H...O hydrogen bonds with iodo-nitro interactions | Acta crystallographica. Section C, Crystal structure communications |
12049500 | 20020613 | Highly active thermomorphic fluorous palladacycle catalyst precursors for the Heck reaction; evidence for a palladium nanoparticle pathway | Organic letters |
Complexity: | 95.1 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 231.93851 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 231.93851 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.7 |
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