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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, [1-(hydroxymethyl)cyclopropyl]-, phenylmethyl ester

OCC1(CC1)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: Carbamic acid, [1-(hydroxymethyl)cyclopropyl]-, phenylmethyl ester
CAS Number: 103500-22-7
Product Number: AG0038CU(AGN-PC-03LJ9V)
Synonyms:
MDL No:
Molecular Formula: C12H15NO3
Molecular Weight: 221.2524

Identification/Properties

Computed Properties
Molecular Weight:
221.256g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
221.105g/mol
Monoisotopic Mass:
221.105g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
245
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


Benzyl (1-(hydroxymethyl)cyclopropyl)carbamate, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various complex molecules and compounds. $name$ can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to undergo selective reactions and introduce functional groups with precision. Its incorporation in synthetic pathways enables chemists to access diverse molecular frameworks with tailored properties, paving the way for the development of novel materials and bioactive substances. By leveraging the synthetic potential of $name$, researchers can explore innovative strategies in drug discovery, materials science, and molecular design, driving advancements in the field of chemistry.