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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
mp
225 °C (dec.) (lit.)
SMILES string
Oc1ccc(c2C(=O)c3c(ccc(O)c3C(=O)c12)[N+]([O-])=O)[N+]([O-])=O
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
InChI key
GJCHQJDEYFYWER-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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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