367834
1,4-二氨基蒽醌
technical grade, ≥88.0%
别名:
1,4-Diamino-9,10-anthracenedione, 1,4-Diamino-9,10-anthraquinone
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关于此项目
经验公式（希尔记法）:
C14H10N2O2
化学文摘社编号:
分子量:
238.24
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
204-922-6
Beilstein/REAXYS Number:
2216556
MDL number:
InChI key
FBMQNRKSAWNXBT-UHFFFAOYSA-N
InChI
1S/C14H10N2O2/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6H,15-16H2
SMILES string
Nc1ccc(N)c2C(=O)c3ccccc3C(=O)c12
grade
technical grade
assay
≥88.0%
mp
265-269 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
644.0 °F - closed cup
flash_point_c
340 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Jonathan P May et al.
Chemical communications (Cambridge, England), (8)(8), 970-971 (2003-05-15)
A novel, long-wavelength, non-fluorescent quencher (LQ), based on 1,4-diaminoanthraquinone, has been incorporated at the 3' and 5'-termini of oligonucleotides. The quencher has been used in Molecular beacons, efficiently quenching the long wavelength fluorophore, Cy5.
Giorgio Cozza et al.
Bioorganic & medicinal chemistry letters, 18(20), 5672-5675 (2008-09-19)
In eukaryotes, protein phosphorylation of serine, threonine or tyrosine residues by protein kinases plays an important role in many cellular processes. Members of the protein kinase CK1 family usually phosphorylate residues of serine that are close to other phosphoserine in
Vsevolod Katritch et al.
Journal of medicinal chemistry, 53(4), 1799-1809 (2010-01-26)
The recent progress in crystallography of G-protein coupled receptors opens an unprecedented venue for structure-based GPCR drug discovery. To test efficiency of the structure-based approach, we performed molecular docking and virtual ligand screening (VLS) of more than 4 million commercially
V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(8), 1799-1809 (2005-05-03)
This work deals with the vibrational spectroscopy of 1,4-diaminoanthraquinone (1,4-DAAQ) and 1,5-dichloroanthraquinone (1,5-DCAQ). The mid and far FTIR and FT-Raman spectra were measured in the condensed state. The fundamental vibrational frequencies and intensity of the vibrational bands were evaluated using
The mutagenic effect in bacteriophage T4D of a hair dye, 1,4 diaminoanthraquinone, and of two solvents, dimethylsulfoxide and ethanol.
I Kvelland
Hereditas, 99(2), 209-213 (1983-01-01)
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