(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide
  • CAS No.:132747-20-7
Other grades of this product :
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Basic information
Product Name:(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide
Synonyms:(1S,2S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide;(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-Diazabicyclo2.2.1üheptane dihydrobromide, 98%;(1S,4S)-2,5-DIAZABICYCLO[2.2.1]HEPTANE DIHYDROBROMIDE 97+%;(1S,4S)-2,5-DIAZABICYLO[2.2.1]HEPTANE DIHYDROBROMIDE;2,5-Diazabicyclo[2.2.1]heptane, hydrobromide (1:2), (1S,4S)-
CAS:132747-20-7
MF:C5H12Br2N2
MW:259.97
EINECS:679-970-8
Product Categories:Chiral
Mol File:132747-20-7.mol
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Chemical Properties
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 activity[α]23/D +22°, c = 1 in H2O
Sensitive Hygroscopic
BRN 4258260
CAS DataBase Reference132747-20-7(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
10-21
HS Code 29335990
MSDS Information
ProviderLanguage
ALFA English
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Usage And Synthesis
Chemical PropertiesGrey?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.
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Preparation Products And Raw materials

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