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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenemethanol, 4,5-dimethoxy-2-nitro-

COc1cc([N+](=O)[O-])c(cc1OC)CO Request for Quotation
Chemical Name: Benzenemethanol, 4,5-dimethoxy-2-nitro-
CAS Number: 1016-58-6
Product Number: AG0004Y4(AGN-PC-0JL6ZD)
Synonyms:
MDL No:
Molecular Formula: C9H11NO5
Molecular Weight: 213.1873

Identification/Properties

Properties
MP:
145-148 °C(lit.)
BP:
383.9±37.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Light Sensitive
Computed Properties
Molecular Weight:
213.189g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
213.064g/mol
Monoisotopic Mass:
213.064g/mol
Topological Polar Surface Area:
84.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
217
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4,5-Dimethoxy-2-nitrophenyl)methanol is a versatile compound commonly used in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a valuable building block for the synthesis of various biologically active molecules due to its unique structure and reactivity. In organic synthesis, it can undergo a range of reactions such as esterification, acetylation, and reduction, allowing for the incorporation of functional groups and modification of the molecule's properties. Additionally, (4,5-Dimethoxy-2-nitrophenyl)methanol plays a crucial role in the development of novel compounds with potential applications in drug discovery, material science, and other research areas. Its flexible nature and compatibility with different synthetic strategies make it a valuable tool for chemists seeking to create innovative and complex molecules with tailored properties.