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重要文件

473006

Sigma-Aldrich

(1S,4S)-(+)-2,5-二氮双环[2.2.1]庚烷 二氢溴酸

97%

同義詞:

(1S,4S)-2,5-二氮双环[2.2.1]庚烷 二氢溴酸

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About This Item

經驗公式(希爾表示法):
C5H10N2 · 2HBr
CAS號碼:
分子量::
259.97
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
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化驗

97%

光學活性

[α]23/D +22°, c = 1 in H2O

mp

300 °C (dec.) (lit.)

SMILES 字串

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 密鑰

ISYQWKOXKGJREA-RSLHMRQOSA-N

應用

(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.[1]
  • A precursor in the preparation of diazabicyclo[2.2.1]heptane derivatives as catalysts, which are applicable in the asymmetric catalysis reactions.[2]
  • An organocatalyst in Biginelli reaction of aromatic aldehydes with ethyl acetoacetate and urea.[3]

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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)
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
Melgar-Fernandez R, et al.
European Journal of Organic Chemistry, 2008(4), 655-672 (2008)

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