41774
1,4-Dimethoxynaphthalene
fluorescent marker, ≥99.5% (HPLC)
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About This Item
Empirical Formula (Hill Notation):
C12H12O2
CAS Number:
Molecular Weight:
188.22
EC Number:
233-209-2
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
2048082
MDL number:
InChI key
FWWRTYBQQDXLDD-UHFFFAOYSA-N
InChI
1S/C12H12O2/c1-13-11-7-8-12(14-2)10-6-4-3-5-9(10)11/h3-8H,1-2H3
SMILES string
COc1ccc(OC)c2ccccc12
assay
≥99.5% (HPLC)
fluorescence
λex 318 nm; λem 394 nm in ethanol (1 mg/mL)
suitability
suitable for fluorescence
storage temp.
2-8°C
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Application
1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Cécile Pégurier et al.
Bioorganic & medicinal chemistry, 11(5), 789-800 (2003-01-23)
Amido derivatives 10-18 of the corresponding oxyamines were synthesised as melatoninergic ligands by the reaction of hydroxyphtalimide with the halogeno derivatives or the corresponding alcohols using Mitsunobu reaction conditions. The affinity of the compounds for chicken brain melatonin receptors and
Samik Upadhaya et al.
Cell stem cell, 27(2), 336-345 (2020-06-27)
Adult mammalian hematopoietic stem cells (HSCs) reside in the bone marrow (BM) but can be mobilized into blood for use in transplantation. HSCs interact with BM niche cells that produce growth factor c-Kit ligand (Kitl/SCF) and chemokine CXCL12, and were
M Abdel-Mogib et al.
Die Pharmazie, 57(4), 286-287 (2002-05-10)
Chromatographic separation of an ethanolic extract of rhizomes of Asphodelus tenuifolius Cav. (Asphodelaceae) yielded in addition to beta-sitosterol, stigmasterol and two anthraquinone derivatives, 1,8-dimethoxynaphthalene as well as two new naphthalene derivatives. The new compounds were identified as 2-acetyl-8-methoxy-3-methyl-1-naphthol and 2-acetyl-1,8-dimethoxy-3-methylnaphthalene.
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