3-(4-Hydroxyphenyl)-1-propanol - CAS 10210-17-0
Catalog: |
BB000778 |
Product Name: |
3-(4-Hydroxyphenyl)-1-propanol |
CAS: |
10210-17-0 |
Synonyms: |
4-(3-hydroxypropyl)phenol |
Application: |
3-(4-Hydroxyphenyl)-1-propanol is a reagent in the synthesis of heteroarylmethoxyphenylalkoxyiminoalkylcarboxylic acids as leukotriene biosynthesis inhibitors. |
IUPAC Name: | 4-(3-hydroxypropyl)phenol |
Description: | 3-(4-Hydroxyphenyl)-1-propanol comes from the fruits of Zanthoxylum cuspidatum. |
Molecular Weight: | 152.19 |
Molecular Formula: | C9H12O2 |
Canonical SMILES: | C1=CC(=CC=C1CCCO)O |
InChI: | InChI=1S/C9H12O2/c10-7-1-2-8-3-5-9(11)6-4-8/h3-6,10-11H,1-2,7H2 |
InChI Key: | NJCVPQRHRKYSAZ-UHFFFAOYSA-N |
Boiling Point: | 311.6 °C at 760 mmHg |
Melting Point: | 55 °C |
Purity: | > 95 % |
Density: | 1.129 g/cm3 |
Solubility: | Sealed in dry, Room Temperature |
Appearance: | Oil |
Storage: | Sealed in dry, Room Temperature |
MDL: | MFCD00002953 |
LogP: | 1.31710 |
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-112812287-A | Method for preparing polycarbonate by ionic liquid catalysis | 20210104 |
JP-2021157049-A | Positive dry film resist | 20200327 |
CN-111205448-A | Method for preparing polycarbonate by catalysis | 20200114 |
CN-111205448-B | Method for preparing polycarbonate by catalysis | 20200114 |
JP-2021110876-A | Positive dry film resist and etching method | 20200114 |
PMID | Publication Date | Title | Journal |
16689671 | 20060501 | Autoradiographic analysis of mouse brain kinin B1 and B2 receptors after closed head trauma and ability of Anatibant mesylate to cross the blood-brain barrier | Journal of neurotrauma |
11778885 | 20011201 | Evidence of a new biotransformation pathway of p-coumaric acid into p-hydroxybenzaldehyde in Pycnoporus cinnabarinus | Applied microbiology and biotechnology |
11167668 | 20010101 | Potent inhibition of CYP2D6 by haloperidol metabolites: stereoselective inhibition by reduced haloperidol | British journal of clinical pharmacology |
Complexity: | 95.7 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 152.083729621 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 152.083729621 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 40.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.3 |
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