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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, 2-chloro-4-hydroxy-5-methoxy-

COc1cc(C=O)c(cc1O)Cl Request for Quotation
Chemical Name: Benzaldehyde, 2-chloro-4-hydroxy-5-methoxy-
CAS Number: 18268-76-3
Product Number: AG00241W(AGN-PC-0JKKFX)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO3
Molecular Weight: 186.5924

Identification/Properties

Computed Properties
Molecular Weight:
186.591g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
186.008g/mol
Monoisotopic Mass:
186.008g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
162
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-hydroxy-5-methoxybenzaldehyde, also known as $name$, plays a critical role in chemical synthesis as a versatile building block. It is commonly utilized in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds due to its unique chemical properties.$name$ is often employed as a key intermediate in the production of biologically active molecules, such as antiviral drugs and antibacterial agents. Its functional groups allow for strategic derivatization, enabling chemists to introduce specific substituents to modulate the activity and properties of the final compound.In addition, $name$ serves as a valuable starting material for the synthesis of natural products and complex heterocyclic compounds. Its reactivity towards various reagents and catalysts makes it a valuable tool for designing efficient synthetic routes towards target molecules with diverse applications.Overall, 2-Chloro-4-hydroxy-5-methoxybenzaldehyde is an indispensable component in the toolkit of synthetic chemists, enabling the construction of molecular architectures with tailored properties and functionalities.