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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)-

2-chloro-4-(cyclopropylmethoxy)benzoic acid

OC(=O)c1ccc(cc1Cl)OCC1CC1 Request for Quotation
Chemical Name: 2-chloro-4-(cyclopropylmethoxy)benzoic acid
CAS Number: 1237084-18-2
Product Number: AG000KZF(AGN-PC-0EYJNO)
Synonyms:
MDL No: MFCD17256604
Molecular Formula: C11H11ClO3
Molecular Weight: 226.6562

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-(cyclopropylmethoxy)benzoic Acid, also known as $name$, plays a pivotal role in chemical synthesis as a versatile building block. This compound is utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and organic compounds. Its unique structure, combining a chloro-substituted benzene ring with a cyclopropylmethoxy group, offers a range of reactivity that enables diversification in synthetic pathways.In chemical synthesis, 2-Chloro-4-(cyclopropylmethoxy)benzoic Acid serves as a valuable starting material for generating complex organic molecules through functional group transformations. Its chloro and cyclopropylmethoxy moieties can undergo substitution, addition, or elimination reactions to introduce different substituents or modify the core structure. Additionally, the presence of the benzoic acid scaffold provides a site for further derivatization, allowing for the creation of new compounds with desired properties.Furthermore, this compound is employed in the synthesis of bioactive compounds and pharmaceutical agents due to its ability to serve as a scaffold for drug design. By manipulating its chemical structure through synthetic routes, researchers can access novel molecules with potential therapeutic applications. The unique combination of functional groups in 2-Chloro-4-(cyclopropylmethoxy)benzoic Acid offers synthetic chemists a valuable tool for designing and accessing diverse chemical entities with targeted biological activities.