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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)-

methyl 2-chloro-1,3-oxazole-4-carboxylate

COC(=O)c1coc(n1)Cl Request for Quotation
Chemical Name: methyl 2-chloro-1,3-oxazole-4-carboxylate
CAS Number: 934236-35-8
Product Number: AG00GUWL(AGN-PC-00Z4XL)
Synonyms:
MDL No:
Molecular Formula: C5H4ClNO3
Molecular Weight: 161.5432

Identification/Properties

Computed Properties
Molecular Weight:
161.541g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
160.988g/mol
Monoisotopic Mass:
160.988g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
141
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-chlorooxazole-4-carboxylate is a versatile reagent commonly used in chemical synthesis as a key building block for the preparation of various organic compounds. Through its unique chemical properties, this compound plays a crucial role in the creation of pharmaceuticals, agrochemicals, and materials with diverse applications in industries such as healthcare, agriculture, and advanced materials. Its ability to undergo selective reactions and form new chemical bonds makes it an essential tool for chemists and researchers seeking efficient routes in the synthesis of complex molecules. By incorporating Methyl 2-chlorooxazole-4-carboxylate into synthetic pathways, chemists can access a wide range of structurally diverse compounds with potential biological activities and functional properties. This compound serves as a valuable scaffold for the development of novel molecules with enhanced properties, making it a valuable asset in the field of organic chemistry and drug discovery.