2-Methyl-1-naphthol - CAS 7469-77-4
Catalog: |
BB035138 |
Product Name: |
2-Methyl-1-naphthol |
CAS: |
7469-77-4 |
Synonyms: |
2-methylnaphthalen-1-ol |
IUPAC Name: | 2-methylnaphthalen-1-ol |
Description: | 2-Methyl-1-naphthol (CAS# 7469-77-4) is a useful research chemical compound. |
Molecular Weight: | 158.20 |
Molecular Formula: | C11H10O |
Canonical SMILES: | CC1=C(C2=CC=CC=C2C=C1)O |
InChI: | InChI=1S/C11H10O/c1-8-6-7-9-4-2-3-5-10(9)11(8)12/h2-7,12H,1H3 |
InChI Key: | SRJCJJKWVSSELL-UHFFFAOYSA-N |
Boiling Point: | 304.3 °C at 760 mmHg |
Density: | 1.144 g/cm3 |
MDL: | MFCD00003964 |
LogP: | 2.85380 |
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, P310, P312, P321, P332+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113426484-A | Catalyst for preparing alpha-tetralone by catalytic oxidation and preparation method and application thereof | 20210719 |
CN-113336656-A | Method for synthesizing propranolol hydrochloride | 20210528 |
CN-113264806-A | Method for preparing tetrahydronaphthalene, cis-decalin and trans-decalin by naphthalene hydrogenation | 20210525 |
CN-112961034-A | Clean production process of naphthol by taking sulfur trioxide as raw material | 20210223 |
CN-112979427-A | Process for synthesizing naphthol through sulfur trioxide indirect sulfonation reaction | 20210223 |
PMID | Publication Date | Title | Journal |
22797675 | 20120828 | Selective synthesis of vitamin K3 over mesoporous NbSBA-15 catalysts synthesized by an efficient hydrothermal method | Dalton transactions (Cambridge, England : 2003) |
21913639 | 20111027 | Mechanistic insights into oxidation of 2-methyl-1-naphthol with dioxygen: autoxidation or a spin-forbidden reaction? | The journal of physical chemistry. B |
19702257 | 20090917 | Influence of an intermolecular charge-transfer state on excited-state relaxation dynamics: solvent effect on the methylnaphthalene-oxygen system and its significance for singlet oxygen production | The journal of physical chemistry. A |
16557330 | 20060407 | Synthesis and biological activity of tetralone abscisic acid analogues | Organic & biomolecular chemistry |
11482669 | 20010801 | Sorption of 1-naphthol to soil and geologic samples with varying diagenetic properties | Chemosphere |
Complexity: | 155 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 158.073164938 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 158.073164938 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.2 |
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