W501506
2-糠酸
≥97%
别名:
呋喃-2-羧酸
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关于此项目
经验公式（希尔记法）:
C5H4O3
化学文摘社编号:
分子量:
112.08
EC Number:
201-803-0
UNSPSC Code:
12164502
Flavis number:
13.136
Beilstein/REAXYS Number:
110149
MDL number:
InChI key
SMNDYUVBFMFKNZ-UHFFFAOYSA-N
InChI
1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)
SMILES string
OC(=O)c1ccco1
assay
≥97%
bp
230-232 °C (lit.)
mp
128-132 °C (lit.)
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Features and Benefits
无味
Other Notes
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flash_point_f
282.7 °F - closed cup
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1C
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_c
139.3 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
[Secondary metabolites of a marine actinomycete Streptomyces sp. (No. 195-02) from South China Sea].
Chun-Yuan Li et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 31(5), 645-647 (2008-10-02)
The metabolites of a marine streptomyces sp. actinomycete (No. 195-02) were studied and eight compounds were isolated from the fermentation liquid, structures were elucidated by spectroscopy methods as p-hydroxy-benzonitrile (1), 2-methyl-furan-3-carboxylic acid(2), furan-2-carboxylic acid (3), cyclo(Phe-Phe) (4), cyclo(Leu-Ileu) (5), nicotinic
María C Rodríguez-Argüelles et al.
Journal of inorganic biochemistry, 103(1), 35-42 (2008-10-25)
Cobalt, nickel, copper and zinc coordination compounds of two thiosemicarbazones with general composition ML(2) (L: monodeprotonated ligand corresponding to 2-acetyl-gamma-butyrolactone thiosemicarbazone, HL(1), and 2-furancarbaldehyde thiosemicarbazone, HL(2)) and also complexes with general composition MCl(2)(HL(2)) were synthesized (except [NiCl(2)(HL(2))] and [Co(L(2))(2)]). The
Hiroshi Yanagita et al.
Bioorganic & medicinal chemistry, 19(2), 816-825 (2011-01-05)
Rapid emergence of drug-resistant variants is one of the most serious problems in chemotherapy for HIV-1 infectious diseases. Inhibitors acting on a target not addressed by approved drugs are of great importance to suppress drug-resistant viruses. HIV-1 reverse transcriptase has
Z B Tan et al.
Journal of analytical toxicology, 27(1), 43-46 (2003-02-18)
An improved high-performance liquid chromatographic (HPLC) method for the analysis of the metabolite furoic acid in the urine of workers occupationally exposed to furfural is described. The procedure involved an alkaline hydrolysis step followed by solvent extraction using ethyl acetate.
Gema Arribas-Lorenzo et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(2), 644-649 (2009-12-17)
5-Hydroxymethylfurfural (HMF) is naturally formed during food processing or cooking activities, giving its ubiquity in the Western diet. HMF could be metabolised to 5-sulfooxymethylfurfural making HMF potentially harmful in an extent unknown at present. Coffee is the main exposure source.
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