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线性分子式:
(O2N)2C6H3CO2H
化学文摘社编号:
分子量:
212.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39032062
UNSPSC Code:
12352100
EC Number:
202-751-1
MDL number:
Beilstein/REAXYS Number:
1914286
产品名称
3,5-二硝基苯甲酸, 99%
InChI key
VYWYYJYRVSBHJQ-UHFFFAOYSA-N
InChI
1S/C7H4N2O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)
SMILES string
OC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
assay
99%
form
solid
mp
204-206 °C (lit.)
solubility
ethanol: soluble 0.5 g/10 mL, clear, yellow to very deep greenish-yellow
functional group
carboxylic acid
nitro
Quality Level
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Application
3,5-二硝基苯甲酸用于树脂的衍生化 和氨苄西林的测定 。
General description
3,5-二硝基苯甲酸与 3,5-二甲基吡啶形成加合物,在室温和 80K 下研究了未氘代和氘代化合物的加合物晶体结构 。它与止痛药物乙醚酰胺形成 1:1 共晶,并以两种多晶型存在 。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - 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, Gloves
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Analytical chemistry, 65(21), 2983-2989 (1993-11-01)
The effect of cross-linking, surface area, and porous nature of modified polystyrene-divinylbenzene (STY-DVB) reagents has been investigated. The supports were prepared via two techniques and modified to contain various chemical functionalities. These reagents were used in an on-line reactor for
The quasi-symmetric OHN and ODN bridges in the adducts of 3, 5-dimethylpyridine with 3, 5-dinitrobenzoic acid.
Jerzykiewicz LB, et al.
Journal of Molecular Structure, 440(1), 175-185 (1998)
Polymorphs and solvates of a cocrystal involving an analgesic drug, ethenzamide, and 3, 5-dinitrobenzoic acid.
Aitipamula S, et al.
Crystal Growth & Design, 10(5), 2229-2238 (2010)
Analytical Letters, 26, 2397-2397 (1993)
Yutaka Tsuji et al.
Journal of the American Chemical Society, 125(50), 15455-15465 (2003-12-11)
Rate constant ratios for addition of the three nucleophilic sites of phenol to the 1-(4-methoxyphenyl)ethyl carbocation (1+) in 50/50 (v/v) trifluoroethanol/water were determined from the relative yields of the three phenol adducts, and absolute rate constants were determined from product
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