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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)-

1,4-Diazabicyclo[3.2.2]nonane

C1NC2CCN(C1)CC2 Request for Quotation
Chemical Name: 1,4-Diazabicyclo[3.2.2]nonane
CAS Number: 283-38-5
Product Number: AG0032ML(AGN-PC-0JQ7U7)
Synonyms:
MDL No:
Molecular Formula: C7H14N2
Molecular Weight: 126.1995

Identification/Properties

Properties
BP:
180 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
126.203g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
126.116g/mol
Monoisotopic Mass:
126.116g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
95.1
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Diazabicyclo[3.2.2]nonane, commonly referred to as DBN, is a powerful and versatile organic base used extensively in chemical synthesis. Its unique structure allows it to act as a non-nucleophilic base, making it particularly valuable in reactions where nucleophilic interference needs to be minimized. DBN is widely employed in organic chemistry as a catalyst for various transformations, such as acylation, alkylation, and condensation reactions. Its ability to efficiently deprotonate a wide range of substrates under mild conditions makes it a popular choice for the synthesis of pharmaceuticals, agrochemicals, and advanced materials. DBN's high reactivity and selectivity have also led to its use in the synthesis of complex natural products and functionalized organic compounds. Furthermore, its low toxicity and ease of handling make DBN a preferred reagent in the laboratory for various synthetic procedures.