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线性分子式:
C3H4(CO2H)2
化学文摘社编号:
分子量:
130.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-917-2
Beilstein/REAXYS Number:
1864823
MDL number:
Assay:
97%
InChI key
FDKLLWKMYAMLIF-UHFFFAOYSA-N
InChI
1S/C5H6O4/c6-3(7)5(1-2-5)4(8)9/h1-2H2,(H,6,7)(H,8,9)
SMILES string
OC(=O)C1(CC1)C(O)=O
assay
97%
mp
134-136 °C (lit.)
solubility
methanol: soluble 1 g/10 mL, clear, colorless
functional group
carboxylic acid
Quality Level
General description
环丙烷-1,1-二羧酸是一种二羧酸。1-氨基环丙烷-1-羧酸氧化酶抑制剂环丙烷-1,1-二羧酸在圣女果中通过HPLC-电喷雾串联质谱法定量。环丙烷-1,1-二羧酸的晶体和分子结构 有酸的报道。
Application
以环丙烷-1,1-二羧酸为原料,合成了含噻二唑和 1,2,4-三唑基团的环丙烷二羧酸杂环衍生物。也用于制备螺-环丙基金属环。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
The crystal and molecular structure of cyclopropane-1, 1-dicarboxylic acid.
Meester MAM, et al.
Acta Crystallographica Section B, Structural Science, 27(3), 630-634 (1971)
Tetrahedron, 45, 1219-1219 (1989)
Nora A Foroud et al.
Phytopathology, 109(5), 796-803 (2018-12-13)
Plant signaling hormones such as ethylene have been shown to affect the host response to various pathogens. Often, the resistance responses to necrotrophic fungi are mediated through synergistic interactions of ethylene (ET) with the jasmonate signaling pathway. On the other
Paolo Ingallinella et al.
Biochemistry, 41(17), 5483-5492 (2002-04-24)
Serine proteases are the most studied class of proteolytic enzymes and a primary target for drug discovery. Despite the large number of inhibitors developed so far, very few make contact with the prime site of the enzyme, which constitutes an
A Hussain K Sharba et al.
Molecules (Basel, Switzerland), 10(9), 1153-1160 (2007-11-17)
New heterocyclic derivatives of cyclopropane dicarboxylic acid comprising thiadiazole and 1,2,4-triazole moieties are reported. Reaction of 1,1-cyclopropane dicarboxylic acid (1) with thiosemicarbazide and phosphorous oxychloride resulted in 1,1-bis (2-amino-1,3,4-thiadiazol-5- yl)cyclopropane (2). Cyclopropane dicarboxylic acid thiosemicarbazide (6) was converted into 1,1-bis(3-thio-4H-1,2,4-triazol-5-yl)
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