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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-Propenoic acid, 3-(2-chlorophenyl)-, (2E)-

OC(=O)/C=C/c1ccccc1Cl Request for Quotation
Chemical Name: 2-Propenoic acid, 3-(2-chlorophenyl)-, (2E)-
CAS Number: 939-58-2
Product Number: AG006AOT(AGN-PC-0ONRY4)
Synonyms:
MDL No:
Molecular Formula: C9H7ClO2
Molecular Weight: 182.6037

Identification/Properties

Properties
MP:
212℃
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(E)-3-(2-Chlorophenyl)acrylic acid, also known as (Z)-2-Chloro-3-phenyl acrylate, serves as a versatile building block in chemical synthesis. This compound is commonly employed in the creation of novel pharmaceuticals, agrochemicals, and fine chemicals due to its structural properties and reactivity.In organic synthesis, (E)-3-(2-Chlorophenyl)acrylic acid can be utilized as a key intermediate in the production of various biologically active compounds. Its presence in the molecule imparts specific functional characteristics, influencing the target compound's properties and behavior. By strategically incorporating this compound into the synthesis pathway, chemists can manipulate its chemical structure to achieve desired molecular properties.Furthermore, (E)-3-(2-Chlorophenyl)acrylic acid can participate in a variety of chemical reactions, such as nucleophilic addition, acylation, and condensation reactions. This versatility allows chemists to modify the compound's structure through controlled chemical transformations, enabling the synthesis of diverse organic compounds with tailored functionalities.Overall, the application of (E)-3-(2-Chlorophenyl)acrylic acid in chemical synthesis underscores its importance as a fundamental building block for the development of innovative compounds with valuable industrial applications.