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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)-

Carbamic acid, ethenyl ester

NC(=O)OC=C Request for Quotation
Chemical Name: Carbamic acid, ethenyl ester
CAS Number: 15805-73-9
Product Number: AG001PYC(AGN-PC-0JKJGZ)
Synonyms:
MDL No:
Molecular Formula: C3H5NO2
Molecular Weight: 87.0773

Identification/Properties

Computed Properties
Molecular Weight:
87.078g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
87.032g/mol
Monoisotopic Mass:
87.032g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
69.2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Vinyl carbamate, a versatile chemical compound, finds wide-ranging applications in chemical synthesis. Its reactivity and unique properties make it a valuable building block in the creation of various organic compounds. In organic synthesis, vinyl carbamate serves as a key intermediate in the preparation of diverse functional groups, such as amines, ketones, and alcohols. Its ability to undergo various reactions, including cycloaddition, elimination, and substitution reactions, provides chemists with a powerful tool for designing and creating complex molecular structures. By harnessing the reactivity of vinyl carbamate, researchers can efficiently access a diverse array of compounds with tailored properties for applications in pharmaceuticals, materials science, and agrochemicals.