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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)-

cis-3-Boc-3,7-diazabicyclo[4.2.0]octane

O=C(N1CC[C@H]2[C@@H](C1)CN2)OC(C)(C)C Request for Quotation
Chemical Name: cis-3-Boc-3,7-diazabicyclo[4.2.0]octane
CAS Number: 1250993-51-1
Product Number: AG000N58(AGN-PC-0WACRO)
Synonyms:
MDL No: MFCD20134217
Molecular Formula: C11H20N2O2
Molecular Weight: 212.2887

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
212.293g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
212.152g/mol
Monoisotopic Mass:
212.152g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
260
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


cis-3-Boc-3,7-diazabicyclo[4.2.0]octane, commonly known as Boc-DABCO, is a versatile compound widely utilized in chemical synthesis as a highly effective organic base. Due to its unique structure and properties, Boc-DABCO plays a crucial role in various organic reactions, predominantly in the realm of heterocyclic and peptide synthesis.This compound is particularly valued for its ability to catalyze a variety of transformations, including cyclization reactions, amidation, and deprotection of functional groups. Additionally, Boc-DABCO is often employed as a stabilizing agent in the synthesis of sensitive compounds due to its inertness and compatibility with a wide range of functional groups.In peptide synthesis, Boc-DABCO serves as a valuable reagent for promoting efficient peptide bond formation and facilitating solid-phase peptide synthesis. Its use in heterocyclic chemistry is also noteworthy, as it aids in the construction of diverse ring systems with high selectivity and efficiency.Overall, cis-3-Boc-3,7-diazabicyclo[4.2.0]octane is an indispensable tool in the arsenal of synthetic chemists, enabling the rapid and controlled synthesis of complex molecules with precision and reliability.