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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)-

Benzaldehyde, 5-chloro-2-hydroxy-3-methyl-

O=Cc1cc(Cl)cc(c1O)C Request for Quotation
Chemical Name: Benzaldehyde, 5-chloro-2-hydroxy-3-methyl-
CAS Number: 23602-63-3
Product Number: AG002NVR(AGN-PC-0KKW3L)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO2
Molecular Weight: 170.5930

Identification/Properties

Properties
MP:
67 °C
BP:
244.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.592g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
170.013g/mol
Monoisotopic Mass:
170.013g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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


5-Chloro-2-hydroxy-3-methylbenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various reactions due to its unique properties and functional groups.In chemical synthesis, $name$ is often employed as a key building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its aldehyde group enables it to participate in important reactions such as aldol condensation, Cannizzaro reaction, and Wittig reaction. Additionally, the chloro and hydroxyl groups present in $name$ offer opportunities for further derivatization and functionalization, allowing chemists to tailor the molecule for specific applications.One common application of 5-Chloro-2-hydroxy-3-methylbenzaldehyde is in the synthesis of heterocyclic compounds, where it serves as a precursor for the construction of complex ring structures. Its ability to undergo various chemical transformations makes it a valuable tool for the creation of diverse molecular architectures.Overall, the versatility and reactivity of 5-Chloro-2-hydroxy-3-methylbenzaldehyde make it an essential ingredient in the toolbox of synthetic chemists, enabling the efficient and precise construction of intricate molecules with potential applications in medicine, agriculture, and materials science.