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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)-

Hydrogen tribromide, compd. with N,N-dimethyl-4-pyridinamine (1:1)OTHER CA INDEX NAMES:4-Pyridinamine, N,N-dimethyl-, mono(hydrogen tribromide)

CN(c1ccncc1)C.BrBr.Br Request for Quotation
Chemical Name: Hydrogen tribromide, compd. with N,N-dimethyl-4-pyridinamine (1:1)OTHER CA INDEX NAMES:4-Pyridinamine, N,N-dimethyl-, mono(hydrogen tribromide)
CAS Number: 92976-81-3
Product Number: AG003LAQ(AGN-PC-0W2K86)
Synonyms:
MDL No:
Molecular Formula: C7H11Br3N2
Molecular Weight: 362.8876

Identification/Properties

Properties
MP:
129-132℃ (lit.)
BP:
194.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
362.891g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
361.845g/mol
Monoisotopic Mass:
359.847g/mol
Topological Polar Surface Area:
16.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
75
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Dimethylaminopyridinium bromide perbromide is a versatile chemical compound commonly utilized in chemical synthesis for its remarkable oxidizing properties. This compound serves as an efficient source of bromine atoms in various reactions, making it a valuable tool in organic chemistry transformations. Additionally, 4-Dimethylaminopyridinium bromide perbromide is particularly useful in the halogenation of aromatic compounds, enabling the introduction of bromine atoms into specific positions on the aromatic ring. Its high reactivity and selectivity make it a preferred reagent for the synthesis of complex organic molecules with bromine functionalities. In addition, this compound is often employed in the preparation of pharmaceutical intermediates and agrochemicals, showcasing its broad applicability in synthetic chemistry.