Merck
CN

383449

Sigma-Aldrich

色酮-3-甲醛

97%

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别名:
4-氧代-4H-1-苯并吡喃-3-羧醛
Empirical Formula (Hill Notation):
C10H6O3
CAS号:
分子量:
174.15
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

solid

mp

151-153 °C (lit.)

SMILES string

O=CC1=COc2ccccc2C1=O

InChI

1S/C10H6O3/c11-5-7-6-13-9-4-2-1-3-8(9)10(7)12/h1-6H

InChI key

FSMYWBQIMDSGQP-UHFFFAOYSA-N

Gene Information

human ... PTPN1(5770)

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此商品
402168402028402192
3-Formylchromone 97%

Sigma-Aldrich

383449

色酮-3-甲醛

6-Bromo-3-formylchromone 99%

Sigma-Aldrich

402168

6-溴-3-甲酰色酮

2-Amino-3-formylchromone 97%

Sigma-Aldrich

402028

2-氨基-3-甲酰色酮

3-Formyl-6-nitrochromone 99%

Sigma-Aldrich

402192

3-甲酰基-6-硝基色酮

form

solid

form

-

form

-

form

-

mp

151-153 °C (lit.)

mp

190-193 °C (lit.)

mp

249 °C (dec.) (lit.)

mp

157-161 °C (lit.)

Gene Information

human ... PTPN1(5770)

Gene Information

human ... PTPN1(5770)

Gene Information

human ... PTPN1(5770)

Gene Information

human ... PTPN1(5770)

一般描述

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。

应用

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。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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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
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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
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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
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
Siffeen Zehra et al.
Journal of fluorescence, 29(4), 1029-1037 (2019-07-22)
A novel coumarin based Schiff base sensor probe 1, was synthesized and structural elucidation was carried out by FTIR, UV-vis, 1H and 13C NMR and MS spectroscopy. The optical properties of the sensor probe were investigated by employing absorption and

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