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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)-

(1S)-2-(4-tert-butylphenyl)cyclopropane-1-carboxylic acid

OC(=O)C1CC1c1ccc(cc1)C(C)(C)C Request for Quotation
Chemical Name: (1S)-2-(4-tert-butylphenyl)cyclopropane-1-carboxylic acid
CAS Number: 445029-32-3
Product Number: AG00D8JU(AGN-PC-06VLBV)
Synonyms:
MDL No:
Molecular Formula: C14H18O2
Molecular Weight: 218.2915

Identification/Properties

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


The 2-(4-(tert-butyl)phenyl)cyclopropanecarboxylic acid is a versatile compound widely utilized in chemical synthesis. This specific compound plays a crucial role in synthetic chemistry due to its unique structural properties. One of the key applications of 2-(4-(tert-butyl)phenyl)cyclopropanecarboxylic acid is its ability to serve as a building block in the synthesis of various biologically active molecules and pharmaceutical intermediates. It can be employed in the construction of complex organic compounds through functional group manipulations, enabling chemists to access a wide range of target molecules with diverse functionalities. The presence of the cyclopropane ring in this compound imparts rigidity and stereochemical control to the synthesized molecules, making it an invaluable tool in the design and production of new chemical entities. Additionally, the tert-butyl substituent enhances the steric hindrance around the cyclopropane ring, influencing the reactivity and selectivity of chemical transformations involving this compound. The versatility and utility of 2-(4-(tert-butyl)phenyl)cyclopropanecarboxylic acid make it a valuable asset in the realm of chemical synthesis, offering chemists the opportunity to explore innovative pathways towards the creation of novel compounds with potential applications in various fields.