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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, 5-chloro-2-hydroxy-

OCc1cc(Cl)ccc1O Request for Quotation
Chemical Name: Benzenemethanol, 5-chloro-2-hydroxy-
CAS Number: 5330-38-1
Product Number: AG00D8PF(AGN-PC-0JLRVE)
Synonyms:
MDL No:
Molecular Formula: C7H7ClO2
Molecular Weight: 158.5823

Identification/Properties

Properties
MP:
90℃
Storage:
Room Temperature;Light sensitive;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
158.581g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
158.013g/mol
Monoisotopic Mass:
158.013g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-(hydroxymethyl)phenol, also known as CHMP, is a versatile compound widely used in chemical synthesis. Its hydroxyl and chloro functional groups make it a valuable building block in various synthetic pathways. In organic chemistry, CHMP is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of different functional groups, enabling chemists to create diverse molecules with specific properties. Additionally, CHMP can act as a ligand in coordination chemistry, participating in metal-catalyzed reactions to facilitate complex transformations. Its role in chemical synthesis extends to the preparation of advanced materials like polymers and resins, where its hydroxyl group can undergo polymerization reactions. Overall, 4-Chloro-2-(hydroxymethyl)phenol serves as a valuable tool for chemists seeking to design and craft complex molecules for various industrial applications.