P73609
吡咯-2-羧酸
99%
别名:
吡咯-2-羧酸
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关于此项目
经验公式（希尔记法）:
C5H5NO2
化学文摘社编号:
分子量:
111.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-221-9
Beilstein/REAXYS Number:
80825
MDL number:
Assay:
99%
Form:
powder
InChI
1S/C5H5NO2/c7-5(8)4-2-1-3-6-4/h1-3,6H,(H,7,8)
InChI key
WRHZVMBBRYBTKZ-UHFFFAOYSA-N
SMILES string
OC(=O)c1ccc[nH]1
assay
99%
form
powder
mp
204-208 °C (dec.) (lit.)
Quality Level
Application
用于合成缩胆囊肽拮抗剂、苯并吡喃抗高血压药和氮杂卓二酮。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - 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, Gloves
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Journal of medicinal chemistry, 33(9), 2667-2672 (1990-09-01)
The synthesis and antihypertensive activity of a series of novel 4-(substituted-carbonylamino)-2H-1-benzopyran-3-ols, administered orally to conscious spontaneously hypertensive rats, are described. Optimum activity was observed for compounds with alkyl, amino, or aryl groups flanking the carbonyl group. Of the alkyl and
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Stress biomarkers such as hormones and neurotransmitters in bodily fluids can indicate an individual's physical and mental state, as well as influence their quality of life and health. Thus, sensitive and rapid detection of stress biomarkers (e.g., cortisol) is important
Conversion of pyrrole to pyrrole-2-carboxylate by cells of Bacillus megaterium in supercritical CO2.
T Matsuda et al.
Chemical communications (Cambridge, England), (21)(21), 2194-2195 (2002-09-21)
Pyrrole was converted to pyrrole-2-carboxylate in supercritical CO2 using cells of Bacillus megaterium PYR 2910, and the yield of the carboxylation reaction in supercritical CO2 was 12 times higher than that under atmospheric pressure.
Benjamin R Clark et al.
Organic & biomolecular chemistry, 9(18), 6306-6311 (2011-07-28)
The biosynthesis of the pyrrolyl moiety of the fungal metabolite rumbrin originates from pyrrole-2-carboxylic acid. In an effort to produce novel derivatives with enhanced biological activity a series of substituted pyrrole-2-carboxylates were synthesised and incubated with the producing organism, Auxarthron
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