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(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide structure

CAS No:
132747-20-7
Formula:
C5H12Br2N2
Chemical 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)-

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Description

Greypowder

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Basic Attributes

Molecular Weight：

259.97

Exact Mass：

259.93467

BRN：

4258260

EC Number：

679-970-8

Color/Form：

White to Light yellow to Light orange

HScode：

29335990

Characteristics

Melting Point：

300 °C (dec.)(lit.)

Critical Temperature & Pressure：

Sealed in dry,Room Temperature

Safety Information

wgk germany：

safety instructions：

22-24/25

GHS Classification：

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 5 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide Use and Manufacturing

(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.

(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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Guide of (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide

Description
Basic Attributes
Characteristics
Safety Information
Use and Manufacturing
Learn More Other Chemicals

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