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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, [[(1,1-dimethylethoxy)carbonyl]carbonimidoyl]bis-,bis(1,1-dimethylethyl) ester

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Chemical Name: Carbamic acid, [[(1,1-dimethylethoxy)carbonyl]carbonimidoyl]bis-,bis(1,1-dimethylethyl) ester
CAS Number: 216584-22-4
Product Number: AG003SH5(AGN-PC-0QY7I6)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
359.423g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
359.206g/mol
Monoisotopic Mass:
359.206g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
504
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N',N''-Tri-boc-guanidine is a versatile compound that finds significant utility in the field of chemical synthesis. As a highly efficient building block, N,N',N''-Tri-boc-guanidine is commonly employed in organic chemistry reactions for the protection of amine groups. Its ability to form stable complexes with amines makes it a valuable tool for safeguarding amine functionalities in complex molecule synthesis. Not only does N,N',N''-Tri-boc-guanidine offer enhanced selectivity, but it also facilitates the manipulation of amine-containing compounds by preventing unwanted side reactions without interfering with the target transformations. Its compatibility with a wide range of reaction conditions and substrates further enhances its appeal as a strategic reagent in chemical synthesis.