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Merck
CN

452653

2,3-二氢-9,10-二羟基-1,4-蒽二酮

90%

别名:

醌茜隐色体

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关于此项目

经验公式(希尔记法):
C14H10O4
化学文摘社编号:
分子量:
242.23
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
241-631-3
MDL number:
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assay

90%

form

solid

mp

154-157 °C (lit.)

SMILES string

Oc1c2C(=O)CCC(=O)c2c(O)c3ccccc13

InChI

1S/C14H10O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-4,17-18H,5-6H2

InChI key

FVXPBEUYCCZFJT-UHFFFAOYSA-N

Other Notes

残留物为醌茜


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

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A comparison of vapour pressure measurements of quinizarin and leuco-quinizarin via transpiration and thermogravimetry
Hinks D, et al.
Coloration Technology, 119(2), 84-90 (2003)
Reactions of 2, 3-dihydro-9, 10-dihydroxy-1, 4-anthracenedione (leucoquinizarin) with hydrazine and substituted hydrazines.
Krapcho AP, et al.
The Journal of Organic Chemistry, 55(16), 4960-4961 (1990)
Gregory I Giles et al.
Journal of peptide science : an official publication of the European Peptide Society, 11(7), 417-423 (2005-01-11)
Anthraquinone peptide derivatives have previously been shown to inhibit the enzyme topoisomerase I (topo I), a pharmaceutical target for the prevention of malignant carcinomas. A highly efficient procedure for the attachment of the anthraquinone moiety to the N-terminus of a