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About This Item
经验公式（希尔记法）:
C12H12O2
CAS号:
分子量:
188.22
Beilstein:
2048082
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
等級
for fluorescence
化驗
≥99.5% (HPLC)
螢光
λex 318 nm; λem 394 nm in ethanol (1 mg/mL)
儲存溫度
2-8°C
SMILES 字串
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 密鑰
FWWRTYBQQDXLDD-UHFFFAOYSA-N
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應用
1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.
包裝
Bottomless glass bottle. Contents are inside inserted fused cone.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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
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
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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