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Merck
모든 사진(1)

주요 문서

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252727

Sigma-Aldrich

Anthraquinone-2-carboxylic acid

98%

동의어(들):

9,10-Dihydro-9,10-dioxo-2-anthracenecarboxylic acid

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C15H8O4
CAS Number:
117-78-2
Molecular Weight:
252.22
EC Number:
204-207-9
MDL number:
MFCD00001231
UNSPSC 코드:
12352100
PubChem Substance ID:
24855233
NACRES:
NA.22

Quality Level

100

분석

98%

양식

solid

mp

287-289 °C (lit.)

작용기

carboxylic acid
ketone

SMILES string

OC(=O)c1ccc2C(=O)c3ccccc3C(=O)c2c1

InChI

1S/C15H8O4/c16-13-9-3-1-2-4-10(9)14(17)12-7-8(15(18)19)5-6-11(12)13/h1-7H,(H,18,19)

InChI key

ASDLSKCKYGVMAI-UHFFFAOYSA-N

관련 카테고리

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCP6057
MKCP6056
MKCJ1545
MKCJ1546
MKCG2229

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리 방문

S Y Tsai et al.
Journal of pharmaceutical sciences, 82(12), 1250-1254 (1993-12-01)
The physicochemical properties of 9,10-anthraquinone-2-carboxylic acid (AQCA) were investigated by thermal analysis, powder X-ray diffraction pattern, solubility, and partition coefficient. The chemical structure of AQCA was confirmed by the data from UV, Fourier transform IR (FTIR), and NMR analyses. Solubility
Coupled Proton and Electron Transfer: Adsorbed Anthraquinone-2-carboxylic Acid Monolayers.
Forster RJ.
Journal of the Electrochemical Society, 144(4), 1165-1173 (1997)
Yiwen Zhu et al.
Materials (Basel, Switzerland), 13(16) (2020-08-17)
Antimicrobial and antiviral materials have attracted significant interest in recent years due to increasing occurrences of nosocomial infections and pathogenic microbial contamination. One method to address this is the combination of photoactive compounds that can produce reactive oxygen species (ROS)
A Bielawska et al.
Folia histochemica et cytobiologica, 39 Suppl 2, 207-208 (2002-02-01)
Although prolidase [E.C.3.4.13.9] is found in normal cells, substantially increased levels are found in some neoplastic tissues. Prolidase evokes the ability to hydrolyse the imido-bond of various low molecular weight compounds coupled to L-proline. The synthesis of three proline analogues
A Bielawska et al.
Roczniki Akademii Medycznej w Bialymstoku (1995), 43, 201-209 (1999-02-11)
The feasibility to targeting prolidase as an antineoplastic prodrug--converting enzyme has been examined. The synthesis of proline analogue of anthraquinone-2-carboxylic acid (potential antineoplastic agent) conjugated through imido-bond (potential target for prolidase action) has been performed. The product was found to
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