2-(3,4-Dimethoxyphenyl)ethanol - CAS 7417-21-2
Catalog: |
BB035009 |
Product Name: |
2-(3,4-Dimethoxyphenyl)ethanol |
CAS: |
7417-21-2 |
Synonyms: |
2-(3,4-dimethoxyphenyl)ethanol |
IUPAC Name: | 2-(3,4-dimethoxyphenyl)ethanol |
Description: | 2-(3,4-Dimethoxyphenyl)ethanol (CAS# 7417-21-2) is a useful research chemical. |
Molecular Weight: | 182.22 |
Molecular Formula: | C10H14O3 |
Canonical SMILES: | COC1=C(C=C(C=C1)CCO)OC |
InChI: | InChI=1S/C10H14O3/c1-12-9-4-3-8(5-6-11)7-10(9)13-2/h3-4,7,11H,5-6H2,1-2H3 |
InChI Key: | SRQAJMUHZROVHW-UHFFFAOYSA-N |
Boiling Point: | 172-174 ℃ (17 mmHg) |
Density: | 1.086 g/cm3 |
Appearance: | Light yellow crystalline powder |
MDL: | MFCD00002894 |
LogP: | 1.23860 |
GHS Hazard Statement: | H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] |
Precautionary Statement: | P264, P280, P305+P351+P338, and P337+P313 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112321402-A | Method for preparing 2-hydroxyethyl phenyl ketone by coupling two components | 20201110 |
CN-112321556-A | Method for preparing alpha, alpha-disubstituted isochroman derivative by three components | 20201110 |
CN-111499498-A | Method for extracting high-purity hydroxytyrosol from fermentation liquor | 20200427 |
CN-111302970-A | Preparation method of 3, 4-dimethoxy benzonitrile | 20200403 |
CN-111302970-B | Preparation method of 3, 4-dimethoxy benzonitrile | 20200403 |
PMID | Publication Date | Title | Journal |
21582580 | 20090325 | 1-(2-Fluoro-phen-yl)-6,7-dimethoxy-isochroman | Acta crystallographica. Section E, Structure reports online |
16050681 | 20050805 | Construction of the benzindenoazepine skeleton via cyclopentannulation of Fischer aminocarbene complexes: total synthesis of bulgaramine | The Journal of organic chemistry |
12857756 | 20031010 | Mechanistic features of lignin peroxidase-catalyzed oxidation of substituted phenols and 1,2-dimethoxyarenes | The Journal of biological chemistry |
11330893 | 20010401 | Structural effects on the OH-promoted fragmentation of methoxy-substituted 1-arylalkanol radical cations in aqueous solution: the role of oxygen acidity | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 138 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 182.094294304 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 182.094294304 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 38.7 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1 |
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