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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, 4-chloro-3-methoxy-

COc1cc(C=O)ccc1Cl Request for Quotation
Chemical Name: Benzaldehyde, 4-chloro-3-methoxy-
CAS Number: 13726-16-4
Product Number: AG00130Q(AGN-PC-00K1I9)
Synonyms:
MDL No: MFCD07787490
Molecular Formula: C8H7ClO2
Molecular Weight: 170.5930

Identification/Properties

Properties
MP:
56-60 °C(lit.)
BP:
265°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.592g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
170.013g/mol
Monoisotopic Mass:
170.013g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-chloro-3-methoxybenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key building block in the creation of various organic compounds. This compound serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 4-chloro-3-methoxybenzaldehyde acts as a valuable starting material for the production of complex molecules. Its structural properties make it a valuable substrate for a range of reactions, including nucleophilic substitution, condensation, and oxidation processes. By utilizing this compound as a precursor, chemists can efficiently access a diverse array of derivatives with tailored properties and functionalities.Furthermore, 4-chloro-3-methoxybenzaldehyde plays a significant role in medicinal chemistry, where it serves as a key component in the synthesis of pharmaceutical drugs. Its presence in the molecular structure of pharmaceutical compounds can impart specific biological activities and enhance their efficacy. Additionally, this compound can be employed in the development of agrochemical products, such as herbicides and insecticides, where its chemical properties contribute to the desired pesticidal activity.Overall, the strategic utilization of 4-chloro-3-methoxybenzaldehyde in chemical synthesis enables the efficient construction of diverse organic molecules with applications across various industries. Its versatility and importance as a synthetic building block underscore its value in advancing research and development efforts in the field of chemistry.