2-Hydroxy-4-methoxybenzaldehyde - CAS 673-22-3
Catalog: |
BB033247 |
Product Name: |
2-Hydroxy-4-methoxybenzaldehyde |
CAS: |
673-22-3 |
Synonyms: |
2-hydroxy-4-methoxybenzaldehyde |
Application: |
2-Hydroxy-4-methoxybenzaldehyde is a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors. |
IUPAC Name: | 2-hydroxy-4-methoxybenzaldehyde |
Description: | 2-Hydroxy-4-methoxybenzaldehyde (CAS# 673-22-3) is a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors. |
Molecular Weight: | 152.15 |
Molecular Formula: | C8H8O3 |
Canonical SMILES: | COC1=CC(=C(C=C1)C=O)O |
InChI: | InChI=1S/C8H8O3/c1-11-7-3-2-6(5-9)8(10)4-7/h2-5,10H,1H3 |
InChI Key: | WZUODJNEIXSNEU-UHFFFAOYSA-N |
Boiling Point: | 271.5 °C |
Purity: | > 98 % |
Density: | 1.231 g/cm3 |
Appearance: | Powder |
MDL: | MFCD00003327 |
LogP: | 1.21330 |
Quality Standard: | Enterprise Standard |
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-113333025-A | Catalyst for preparing all-trans beta-carotene and preparation method and application thereof | 20210628 |
CN-113201233-A | Photochromic organic pigment and preparation method thereof | 20210429 |
CN-113200970-A | Osthole isoxazoline derivatives, and preparation method and application thereof | 20210426 |
CN-112939916-A | Method for synthesizing coumarin-3-carboxylic acid compounds by one-pot two-step method | 20210317 |
CN-113024499-A | Green synthesis method of coumarin-3-carboxylic acid compounds | 20210317 |
PMID | Publication Date | Title | Journal |
22609460 | 20120701 | Shikimate pathway modulates the elicitor-stimulated accumulation of fragrant 2-hydroxy-4-methoxybenzaldehyde in Hemidesmus indicus roots | Plant physiology and biochemistry : PPB |
22412575 | 20120301 | N'-(2-Hy-droxy-4-meth-oxy-benzyl-idene)-4-methyl-benzohydrazide | Acta crystallographica. Section E, Structure reports online |
21815721 | 20120101 | Insecticidal activity of the root bark essential oil of Periploca sepium Bunge and its main component | Natural product research |
21837453 | 20120101 | Modification of gold nanoparticle loaded on activated carbon with bis(4-methoxysalicylaldehyde)-1,2-phenylenediamine as new sorbent for enrichment of some metal ions | Biological trace element research |
22221363 | 20120101 | Food protective effects of Periploca sepium oil and its active component against stored food mites | Journal of food protection |
Complexity: | 135 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 152.047344113 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 152.047344113 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 46.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.5 |
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