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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, 2-(chloromethyl)-, methyl ester

COC(=O)C(=C)CCl Request for Quotation
Chemical Name: 2-Propenoic acid, 2-(chloromethyl)-, methyl ester
CAS Number: 922-15-6
Product Number: AG00GUK9(AGN-PC-0NIZWF)
Synonyms:
MDL No:
Molecular Formula: C5H7ClO2
Molecular Weight: 134.5609

Identification/Properties

Properties
BP:
156.7°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Liquid
Computed Properties
Molecular Weight:
134.559g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
134.013g/mol
Monoisotopic Mass:
134.013g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
109
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#:
-
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-(chloromethyl)acrylate is a key intermediate in organic synthesis, valued for its versatile applications in chemical reactions. This compound serves as a valuable building block in the synthesis of various advanced materials, pharmaceuticals, and specialized chemicals. In chemical synthesis, Methyl 2-(chloromethyl)acrylate is commonly utilized as a reagent to introduce functional groups onto organic molecules. Its acrylate moiety enables it to participate in radical polymerization reactions, leading to the formation of polymers with tailored structures and properties. Additionally, the chloromethyl group can undergo nucleophilic substitution reactions, allowing for the introduction of substituents or crosslinking functionalities.The presence of both the acrylate and chloromethyl groups in this compound provides a diverse range of synthetic possibilities, making it a valuable tool for chemists seeking to modify or create new compounds with specific properties. Its reactivity and compatibility with a variety of reaction conditions make Methyl 2-(chloromethyl)acrylate a versatile and indispensable compound in modern chemical synthesis strategies.