522546
1,8-Dihydroxy-4,5-dinitroanthraquinone
97%
Synonym(s):
ARDP0006
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About This Item
Empirical Formula (Hill Notation):
C14H6N2O8
CAS Number:
Molecular Weight:
330.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-360-3
MDL number:
Assay:
97%
InChI key
GJCHQJDEYFYWER-UHFFFAOYSA-N
InChI
1S/C14H6N2O8/c17-7-3-1-5(15(21)22)9-11(7)14(20)12-8(18)4-2-6(16(23)24)10(12)13(9)19/h1-4,17-18H
SMILES string
Oc1ccc(c2C(=O)c3c(ccc(O)c3C(=O)c12)[N+]([O-])=O)[N+]([O-])=O
assay
97%
mp
225 °C (dec.) (lit.)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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David A Constant et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(40), 10136-10141 (2018-09-20)
Many positive-strand RNA viruses translate their genomes as single polyproteins that are processed by host and viral proteinases to generate all viral protein products. Among these is dengue virus, which encodes the serine proteinase NS2B/3 responsible for seven different cleavages
Measurement and Correlation of Derivatized Anthraquinone Solubility in Supercritical Carbon Dioxide.
Alwi RS and Tamura K.
Journal of Chemical and Engineering Data, 60(10), 3046-3052 (2015)
Catalysed hydrogenation of hydroxynitroanthraquinones in strong acid.
Morley JO and Hutcheson R.
Journal of Chemical Technology and Biotechnology, 30(1), 409-414 (1980)
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