D108200
2,5-二羟基苯甲醛
98%
别名:
龙胆醛
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关于此项目
线性分子式:
(HO)2C6H3CHO
化学文摘社编号:
分子量:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-789-6
Beilstein/REAXYS Number:
1363961
MDL number:
Assay:
98%
Form:
crystals
产品名称
2,5-二羟基苯甲醛, 98%
InChI key
CLFRCXCBWIQVRN-UHFFFAOYSA-N
InChI
1S/C7H6O3/c8-4-5-3-6(9)1-2-7(5)10/h1-4,9-10H
SMILES string
Oc1ccc(O)c(C=O)c1
assay
98%
form
crystals
mp
97-99 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
N A Santagati et al.
Journal of pharmaceutical and biomedical analysis, 29(6), 1105-1111 (2002-07-12)
A method was developed for the analysis of primary aliphatic amines by high performance liquid chromatography coupled with electrochemical detector. The electrochemical oxidation of aliphatic amines derivatized with 2,5-dihydroxybenzaldehyde was investigated at porous graphite electrodes. The derivatization reactions were performed
Gobind S Bisht et al.
Langmuir : the ACS journal of surfaces and colloids, 28(39), 14055-14064 (2012-09-06)
We report on the functionalization of a micropatterned carbon electrode fabricated using the carbon-MEMS process for its use as a miniature diffusion-free glucose oxidase anode. Carbon-MEMS based electrodes offer precise manufacturing control on both the micro- and nanoscale and possess
Javed Iqbal et al.
Organic letters, 14(2), 552-555 (2012-01-06)
Functionalized β-aryl alanine ester derivatives were found to undergo rapid C-N and C-O bond formation with quinol carbonyl compounds to afford 2H-benzo[b][1,4]oxazines in good to excellent yields. This unprecedented finding reported herein offers a straightforward, highly efficient, and rapid method
S Rauli et al.
Journal of biochemistry, 123(5), 918-923 (1998-06-19)
Measurement of the concentrations of aldehydes in biological samples has become the object of much effort due to their relevance in relation to the toxic effects of lipid peroxidation, through which a number of aldehydes are derived. We have reconsidered
Virginia Delgado et al.
Molecules (Basel, Switzerland), 18(1), 721-734 (2013-01-10)
A variety of phenylaminoisoquinolinequinones were synthesized and tested for their antiproliferative activity against three human-tumor derived cancer cell lines. The new aminoquinones were prepared from 4-methoxycarbonyl-3-methylisoquinoline-5,8-quinone (1) via acid-induced amination and bromination reactions. Remarkable differences in antiproliferative activity were observed
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