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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, 2-chloro-5-nitro-

OCc1cc(ccc1Cl)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenemethanol, 2-chloro-5-nitro-
CAS Number: 80866-80-4
Product Number: AG003GZJ(AGN-PC-0JSTPM)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO3
Molecular Weight: 187.5804

Identification/Properties

Properties
MP:
75-79 °C
BP:
344.1 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
187.579g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
187.004g/mol
Monoisotopic Mass:
187.004g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
171
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Expertly synthesized, (2-Chloro-5-nitrophenyl)methanol serves as a versatile building block in the realm of chemical synthesis. This compound is a key intermediate in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties and reactivity. Through selective modification of its functional groups, this compound can be transformed into a diverse range of derivatives with tailored properties for specific applications. Its presence in the synthesis process enables the formation of compounds with enhanced biological activity, improved functionality, or targeted physical characteristics. The strategic incorporation of (2-Chloro-5-nitrophenyl)methanol in chemical reactions facilitates the production of complex molecules with precision and efficiency, making it an indispensable component in the arsenal of synthetic chemists.