383449
色酮-3-甲醛
97%
别名:
4-氧代-4H-1-苯并吡喃-3-羧醛
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关于此项目
经验公式（希尔记法）:
C10H6O3
化学文摘社编号:
分子量:
174.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-451-5
MDL number:
产品名称
色酮-3-甲醛, 97%
InChI key
FSMYWBQIMDSGQP-UHFFFAOYSA-N
InChI
1S/C10H6O3/c11-5-7-6-13-9-4-2-1-3-8(9)10(7)12/h1-6H
SMILES string
O=CC1=COc2ccccc2C1=O
assay
97%
form
solid
mp
151-153 °C (lit.)
functional group
aldehyde
ketone
Quality Level
Gene Information
human ... PTPN1(5770)
Application
3-甲酰色原酮可用于以下研究：
- ( E )-3-（2-芳基羰基-3-（芳基氨基）烯丙基）-4 H -色烯-4-酮与 ( E )-3-（二甲氨基）-1-芳基脯氨酸-2-烯-1-酮和苯胺在无催化剂条件下的三组分多米诺反应制备文库。
- 新型铬酮类化合物的合成。
- 3-（2-羟基苯甲酰基）喹啉和 7 H -色胺诺 [3,2- c ] 喹啉-7-酮的合成。
General description
质子化 3-甲酰色原酮 (3-FC) 的电喷雾离子化质谱 (ESI-MS) 显示丢失 H 2 是生成烯酮阳离子的主要裂解途径，与水反应生成质子化羧酸。研究了 3-FC 对亚硝基二乙胺 (NDEA) 介导的早期肝细胞癌变的 体内 有益作用。3-FC 及其衍生物的合成与表征已有报告。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Andrey S Plaskon et al.
The Journal of organic chemistry, 73(15), 6010-6013 (2008-07-03)
A facile and versatile procedure for the synthesis of 3-(2-hydroxybenzoyl)quinolines and 7H-chromeno[3,2-c]quinolin-7-ones was elaborated on the basis of TMSCl-mediated recyclization of 3-formylchromone with various anilines. Limitations and scope of this methodology were established, and a possible mechanism for the heterocyclizations
Muhammed Bilaal Ismail et al.
Nucleosides, nucleotides & nucleic acids, 38(12), 950-971 (2019-07-11)
Herein, we report the DNA interaction studies of rhenium(I) and -(V) compounds with Schiff base chelates encompassing biologically relevant moieties. More specifically, the DNA interaction capabilities of these rhenium complexes were probed using Gel Electrophoresis and Calf Thymus-DNA titrations monitored
Pitchaimani Prasanna et al.
Beilstein journal of organic chemistry, 10, 459-465 (2014-03-13)
The three-component domino reactions of (E)-3-(dimethylamino)-1-arylprop-2-en-1-ones, 3-formylchromone and anilines under catalyst-free conditions afforded a library of novel (E)-3-(2-arylcarbonyl-3-(arylamino)allyl)-4H-chromen-4-ones in good to excellent yields and in a diastereoselective transformation. This transformation generates one C-C and one C-N bond and presumably proceeds
Pedatsur Neta et al.
Rapid communications in mass spectrometry : RCM, 28(17), 1871-1882 (2014-08-05)
Electrospray ionization mass spectrometry (ESI-MS) of many protonated aldehydes shows loss of CO as a major fragmentation pathway. However, we find that certain aldehydes undergo loss of H2 followed by reaction with water in the collision cell. This complicates interpretation
Koichi Takao et al.
Bioorganic chemistry, 83, 432-437 (2018-11-15)
A series of eighteen pyrano[4,3-b][1]benzopyranone derivatives (1a-9b) were synthesized, and structure-activity relationships of their monoamine oxidase (MAO) A and B, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE) inhibitory activities were evaluated. Most of the synthesized compounds exhibited weak inhibitory activity toward MAO-A
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