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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, 3-chloro-2-methoxy-

COc1c(C=O)cccc1Cl Request for Quotation
Chemical Name: Benzaldehyde, 3-chloro-2-methoxy-
CAS Number: 223778-54-9
Product Number: AG00C3VY(AGN-PC-00251G)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO2
Molecular Weight: 170.5930

Identification/Properties

Computed Properties
Molecular Weight:
170.592g/mol
XLogP3:
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:
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


3-Chloro-2-methoxybenzaldehyde, also known as the organic compound with the chemical formula C8H7ClO2, plays a crucial role in chemical synthesis due to its unique properties and versatile applications. One of the primary uses of 3-Chloro-2-methoxybenzaldehyde in chemical synthesis is as a key intermediate in the production of pharmaceuticals. This compound serves as a building block in the synthesis of various drugs and active pharmaceutical ingredients, contributing to the development of new medications.Furthermore, 3-Chloro-2-methoxybenzaldehyde is utilized in the preparation of aromatic compounds through various chemical reactions such as nucleophilic aromatic substitution and Friedel-Crafts acylation. Its distinctive structure allows for selective functionalization, enabling chemists to create complex molecular structures with specific substitution patterns. Additionally, this compound is a valuable reagent in organic synthesis for the modification of natural products and the creation of novel chemical entities with desirable properties.In summary, 3-Chloro-2-methoxybenzaldehyde serves as a versatile and essential component in chemical synthesis, facilitating the creation of pharmaceuticals, aromatic compounds, and customized organic molecules through precise reactions and strategic transformations.