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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, [3-(2-hydroxyethyl)-4-pyridinyl]-, 1,1-dimethylethyl ester

OCCc1c[nH]ccc1=NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, [3-(2-hydroxyethyl)-4-pyridinyl]-, 1,1-dimethylethyl ester
CAS Number: 219834-80-7
Product Number: AG00C2EP(AGN-PC-0NEQXT)
Synonyms:
MDL No: MFCD20491404
Molecular Formula: C12H18N2O3
Molecular Weight: 238.2829

Identification/Properties

Computed Properties
Molecular Weight:
238.287g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
238.132g/mol
Monoisotopic Mass:
238.132g/mol
Topological Polar Surface Area:
71.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
251
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (3-(2-hydroxyethyl)pyridin-4-yl)carbamate is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in various synthetic pathways due to its functional groups and structural features. In organic synthesis, it can act as a protecting group for amines, enabling selective reactions at other functional groups while keeping the amine moiety unaltered. Additionally, the presence of the pyridine ring confers specific reactivity patterns, making it useful for the synthesis of complex organic molecules and pharmaceutical intermediates. Its tert-butyl group provides steric hindrance and can influence the molecule's solubility and stability in different solvents, further expanding its applicability in synthetic chemistry.