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About This Item
Empirical Formula (Hill Notation):
C12H12O2
CAS Number:
Molecular Weight:
188.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
86-90 °C (lit.)
SMILES string
COc1ccc(OC)c2ccccc12
InChI
1S/C12H12O2/c1-13-11-7-8-12(14-2)10-6-4-3-5-9(10)11/h3-8H,1-2H3
InChI key
FWWRTYBQQDXLDD-UHFFFAOYSA-N
Application
1,4-Dimethoxynaphthalene may be used in the preparation of 1,7-dideoxy-3-demethylprekinamycin and 3-acetoxy-2-bromo-1,4-dimethoxynaphthalene.3-acetoxy-2-bromo-1,4-dimethoxynaphthalene
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Novel haloacetoxylation of 1, 4-dimethoxynaphthalenes using hypervalent iodine chemistry.
Evans PA and Brandt TA.
Tetrahedron Letters, 27(36), 6443-6446 (1996)
William Williams et al.
The Journal of organic chemistry, 62(13), 4364-4369 (1997-06-27)
2-(Diazobenzyl)-p-naphthoquinone was synthesized from 2-benzyl-1,4-dimethoxynaphthalene by cerric ammonium nitrate oxidation to 2-benzyl-p-naphthoquinone followed by diazo transfer with tosyl azide. 1,7-Dideoxy-3-demethylprekinamycin was prepared from 1,4-dimethoxynaphthalene by bromination, lithiation, and condensation with acetanthranil to give 2-(2'-N-acetaminobenzoyl)-1,4-dimethoxynaphthalene, which, following deacylation, was subjected to
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