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Merck
CN

343412

Sigma-Aldrich

1,1-环丙烷二羧酸

97%

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About This Item

线性分子式:
C3H4(CO2H)2
CAS号:
分子量:
130.10
Beilstein:
1864823
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

134-136 °C (lit.)

溶解性

methanol: soluble 1 g/10 mL, clear, colorless

官能团

carboxylic acid

SMILES字符串

OC(=O)C1(CC1)C(O)=O

InChI

1S/C5H6O4/c6-3(7)5(1-2-5)4(8)9/h1-2H2,(H,6,7)(H,8,9)

InChI key

FDKLLWKMYAMLIF-UHFFFAOYSA-N

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一般描述

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。

应用

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。

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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分析证书(COA)

Lot/Batch Number

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Tetrahedron, 45, 1219-1219 (1989)
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)
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
Konstantinos Petritis et al.
Phytochemical analysis : PCA, 14(6), 347-351 (2003-12-12)
Varying concentrations of cyclopropane-1,1-dicarboxylic acid (CDA), an inhibitor of 1-aminocyclopropane-1-carboxylic acid oxidase, added to the solid culture medium of tomato nodal shoot segments resulted in a reduction in the level of endogenous ethylene according to the concentration of inhibitor applied.

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