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Merck
CN

T0267

3,4,5,6-四氢邻苯二甲酸酐

≥95%

别名:

1,2-环己烯二羧酸酐

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关于此项目

经验公式(希尔记法):
C8H8O3
化学文摘社编号:
分子量:
152.15
EC Number:
219-374-3
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
136335
MDL number:
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assay

≥95%

mp

69-73 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C1OC(=O)C2=C1CCCC2

InChI

1S/C8H8O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H2

InChI key

HMMBJOWWRLZEMI-UHFFFAOYSA-N



pictograms

Health hazardCorrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1

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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分析证书(COA)

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A Ikai et al.
The Journal of biological chemistry, 265(14), 8280-8284 (1990-05-15)
As a model for the molecular structure of proteins belonging to the alpha 2-macroglobulin family, ovomacroglobulin of reptilian origin was studied by electron microscopy in the original tetrameric form as well as in the dissociated forms into half- and quarter
J B Swaney
Journal of lipid research, 24(3), 245-252 (1983-03-01)
Trypsin digestion of human high density lipoprotein (d 1.125-1.21 g/ml) on which the lysine residues have been masked with the reversible blocking group, 2,3,4,5-tetrahydrophthallic anhydride (THPA), was found to result in the fragmentation of the apoA-I component, but not the
Subat Turdi et al.
Toxicology letters, 178(3), 197-201 (2008-05-10)
Doxorubicin is an effective anthracycline used for cancer therapy. However, the clinical application of doxorubicin has been largely limited by its irreversible cardiotoxicity, which is mainly induced by the primary amine group. In this study, we structurally modified doxorubicin by