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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)-

tert-butyl N-pyrrol-1-ylcarbamate

O=C(Nn1cccc1)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-pyrrol-1-ylcarbamate
CAS Number: 937046-95-2
Product Number: AG006EMU(AGN-PC-086FDV)
Synonyms:
MDL No:
Molecular Formula: C9H14N2O2
Molecular Weight: 182.2197

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
182.223g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
182.106g/mol
Monoisotopic Mass:
182.106g/mol
Topological Polar Surface Area:
43.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
181
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#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl 1H-pyrrol-1-ylcarbamate is a versatile chemical compound commonly used in organic synthesis as a protecting group for amines. This compound plays a crucial role in the realm of chemical synthesis by selectively masking amine functionalities in complex molecules, thereby enabling the manipulation of other reactive sites without interference. Through the strategic incorporation of tert-Butyl 1H-pyrrol-1-ylcarbamate, chemists can precisely control the reactivity of amine groups, facilitating the synthesis of intricate molecular structures with high levels of precision and efficiency. This compound's unique chemical properties make it an indispensable tool in the toolkit of synthetic chemists seeking to construct elaborate organic molecules with tailored functionalities and properties.