| Identification | More | [Name]
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide | [CAS]
132747-20-7 | [Synonyms]
(1S,4S)-2,5-DIAZABICYCLO[2.2.1]HEPTANE 2 HBR
(1S,4S)-(+)-2,5-DIAZABICYCLO[2.2.1]HEPTANE DIHYDROBROMIDE
(1S,4S)-2,5-DIAZABICYCLO[2.2.1]HEPTANE DIHYDROBROMIDE
(1S,2S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide
(1S,4S)-2,5-DIAZABICYLO[2.2.1]HEPTANE DIHYDROBROMIDE
(1S,4S)-2,5-DIAZABICYCLO[2.2.1]HEPTANE DIHYDROBROMIDE 97+%
(1S,2S)-2,5-Diazabicyclo2.2.1üheptane dihydrobromide, 98% | [EINECS(EC#)]
679-970-8 | [Molecular Formula]
C5H12Br2N2 | [MDL Number]
MFCD08272741 | [Molecular Weight]
259.97 | [MOL File]
132747-20-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
300 °C (dec.)(lit.) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder to crystal | [color ]
White to Light yellow to Light orange | [Optical Rotation]
[α]23/D +22°, c = 1 in H2O | [Sensitive ]
Hygroscopic | [BRN ]
4258260 | [InChI]
1S/C5H10N2.2BrH/c1-4-2-6-5(1)3-7-4;;/h4-7H,1-3H2;2*1H/t4-,5-;;/m0../s1 | [InChIKey]
ISYQWKOXKGJREA-RSLHMRQOSA-N | [SMILES]
Br.Br.C1N[C@@H]2CN[C@H]1C2 | [CAS DataBase Reference]
132747-20-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
10-21 | [HS Code ]
29335990 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
Grey?powder | [Uses]
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane Dihydrobromide acts as a reagent for the synthesis and characterization of new piperazine-type inhibitors for mitochondrial ubiquinone reductase, preparation of heterocyclic compounds as chemokine receptor inhibitors useful in treatment of CXCR4-mediated diseases. | [Uses]
(1S,4S)-(+)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide can be used as:
- A starting material for the synthesis of chiral diazabicyclic ligands, applicable in the preparation of dicopper(II) complexes.
- A precursor in the preparation of diazabicyclo[2.2.1]heptane derivatives as catalysts, which are applicable in the asymmetric catalysis reactions.
- An organocatalyst in Biginelli reaction of aromatic aldehydes with ethyl acetoacetate and urea.
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