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Merck

473006

Sigma-Aldrich

(1S,4S)-(+)-2,5-二氮双环[2.2.1]庚烷 二氢溴酸

97%

别名:

(1S,4S)-2,5-二氮双环[2.2.1]庚烷 二氢溴酸

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About This Item

经验公式(希尔记法):
C5H10N2 · 2HBr
分子量:
259.97
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

旋光性

[α]23/D +22°, c = 1 in H2O

mp

300 °C (dec.) (lit.)

SMILES字符串

Br.Br.C1N[C@@H]2CN[C@H]1C2

InChI

1S/C5H10N2.2BrH/c1-4-2-6-5(1)3-7-4;;/h4-7H,1-3H2;2*1H/t4-,5-;;/m0../s1

InChI key

ISYQWKOXKGJREA-RSLHMRQOSA-N

应用

(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.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

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Dicopper (II) complexes of chiral C2-symmetric diamino-bis (2-methylpyridyl) and diamino-bis (2-methylbenzimidazolyl) ligands
Melgar-Fernandez R, et al.
European Journal of Organic Chemistry, 2008(4), 655-672 (2008)
Application of (1S, 4S)-2, 5-diazabicyclo [2.2. 1] heptane derivatives in asymmetric organocatalysis: the Biginelli reaction
Gonzalez-Olvera R, et al.
ARKIVOC (Gainesville, FL, United States), 6(4) (2008)
Dicopper (II) complexes of chiral C2-symmetric diamino-bis (2-methylpyridyl) and diamino-bis (2-methylbenzimidazolyl) ligands
Perez V, et al.
Inorganic Chemistry Communications, 14(2), 389-391 (2011)

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