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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-methoxy-

COc1cc(O)c(cc1Cl)C=O Request for Quotation
Chemical Name: Benzaldehyde, 5-chloro-2-hydroxy-4-methoxy-
CAS Number: 89938-56-7
Product Number: AG003MO7(AGN-PC-0ALJ0T)
Synonyms:
MDL No: MFCD08059080
Molecular Formula: C8H7ClO3
Molecular Weight: 186.5924

Identification/Properties

Computed Properties
Molecular Weight:
186.591g/mol
XLogP3:
2.2
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-4-methoxysalicylaldehyde, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique chemical structure makes it valuable for various applications in organic synthesis. One key application of 5-Chloro-4-methoxysalicylaldehyde is its use as a key intermediate in the preparation of biologically active compounds and pharmaceuticals. Its functional groups allow for easy manipulation, enabling chemists to introduce specific modifications to create new molecules with desired properties. In addition, 5-Chloro-4-methoxysalicylaldehyde serves as a valuable precursor in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry and drug discovery. Its reactivity and compatibility with different functional groups make it a versatile starting material for the production of a wide range of complex molecules. Furthermore, this compound is utilized in the development of agrochemicals, dyes, and other fine chemicals due to its ability to participate in diverse chemical reactions and form intricate structures. Its versatility and synthetic utility make it a valuable asset in the field of chemical synthesis.