120804
邻香草醛
99%
别名:
2-羟基-3-甲氧基苯甲醛, 2-香草醛, 3-甲氧基水杨醛
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关于此项目
线性分子式:
CH3OC6H3-2-(OH)CHO
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-715-3
Beilstein/REAXYS Number:
471913
MDL number:
产品名称
邻香草醛, 99%
InChI key
JJVNINGBHGBWJH-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-7-4-2-3-6(5-9)8(7)10/h2-5,10H,1H3
SMILES string
COc1cccc(C=O)c1O
assay
99%
form
solid
bp
265-266 °C (lit.)
mp
40-42 °C (lit.)
functional group
aldehyde
Quality Level
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Application
o-香兰素已用于研究-香兰素与-甲苯胺之间的无溶剂反应分析。用于合成新的铁（III）和铝（III）配体。
Biochem/physiol Actions
-香兰素诱导脱氧核糖核酸损伤，如彗星试验所检测到的那样。
General description
邻香兰素是一种常用于合成希夫碱配体的基础材料。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup - (External MSDS)
flash_point_c
113 °C - closed cup - (External MSDS)
ppe
dust mask type N95 (US), Eyeshields, Gloves
G Frenzilli et al.
Mutation research, 468(2), 93-108 (2000-07-07)
To validate the alkaline single cell gel (SCG) assay as a tool for the detection of DNA damage in human leukocytes, we investigated the in vitro activity of 18 chemicals. Thirteen of these chemicals (pyrene (PY), benzo(a)pyrene (BaP), cyclophosphamide (CP)
Peter Temitope Adeboye et al.
Scientific reports, 7, 42635-42635 (2017-02-17)
The ability of Saccharomyces cerevisiae to catabolize phenolic compounds remains to be fully elucidated. Conversion of coniferyl aldehyde, ferulic acid and p-coumaric acid by S. cerevisiae under aerobic conditions was previously reported. A conversion pathway was also proposed. In the
Li-Jun Ru et al.
Molecules (Basel, Switzerland), 23(7) (2018-07-14)
A self-assembled ZnII-NdIII heterohexanuclear coordination compound [Zn₄Nd₂(L)₄(bdc)₂]·2NO₃ based on a hexadentate Salamo-like chelating ligand (H₂L = 1,2-bis(3-methoxysalicylideneaminooxy)ethane]) and H₂bdc (H₂bdc = terephthalic acid) has been synthesized and characterized by elemental analyses, IR and UV/Vis spectra, and X-ray crystallography. Two crystallographically
Vanillin and o-vanillin oligomers as models for dendrimer disassembly
Robert K M et al.
New Journal of Science, 36, 492-505 (2012)
Jingqun Gao et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(4), 1278-1286 (2011-02-08)
In this work, three o-Vanillin Schiff Bases (o-VSB: o-Vanillin-D-Phenylalanine (o-VDP), o-Vanillin-L-Tyrosine (o-VLT) and o-Vanillin-L-Levodopa (o-VLL)) with alanine constituent were synthesized by direct reflux method in ethanol solution, and then were used to study the interaction to bovine serum albumin (BSA)
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