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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-4-methyl-

O=Cc1cc(Cl)c(cc1O)C Request for Quotation
Chemical Name: Benzaldehyde, 5-chloro-2-hydroxy-4-methyl-
CAS Number: 3328-68-5
Product Number: AG00BZPN(AGN-PC-0KK7BA)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO2
Molecular Weight: 170.5930

Identification/Properties

Properties
BP:
252.2°C at 760 mmHg
Storage:
Inert atmosphere;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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-2-hydroxy-4-methylbenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique molecular structure facilitates its role as a crucial intermediate in the synthesis of diverse organic compounds.One of the primary applications of 5-Chloro-2-hydroxy-4-methylbenzaldehyde is in the production of pharmaceuticals. Its structural features make it an important precursor in the synthesis of active pharmaceutical ingredients (APIs) for a range of medicinal products. Additionally, this compound is utilized in the development of novel drug molecules with potential therapeutic benefits.In the field of agrochemicals, 5-Chloro-2-hydroxy-4-methylbenzaldehyde is employed for the synthesis of pesticides, herbicides, and fungicides. By incorporating this compound into the chemical structures of agrochemical products, manufacturers can enhance the efficacy and specificity of these agricultural chemicals, contributing to sustainable pest management practices.Furthermore, in the realm of fine chemicals production, 5-Chloro-2-hydroxy-4-methylbenzaldehyde plays a crucial role as a valuable intermediate. Its reactivity and functional groups make it an essential component in the synthesis of specialty chemicals, flavors, fragrances, and other high-value compounds used in various industries.Overall, the versatility and significance of 5-Chloro-2-hydroxy-4-methylbenzaldehyde in chemical synthesis make it a valuable and indispensable compound for the development of advanced materials and innovative products across diverse sectors.