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Merck

684104

Sigma-Aldrich

(1S,2S)-1,2-双(2,4,6-三甲基苯基)乙二胺 二盐酸盐 水合物

95%

别名:

(1S,2S)-1,2-双(2,4,6-三甲基苯基)-1,2-乙二胺 二盐酸盐 水合物

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About This Item

经验公式(希尔记法):
C20H28N2 · 2HCl
分子量:
369.37
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.22

化驗

95%

形狀

solid

光學活性

[α]20/D −129°, c = 1 in H2O

mp

>300 °C

SMILES 字串

Cl.Cl.Cc1cc(C)c([C@H](N)[C@@H](N)c2c(C)cc(C)cc2C)c(C)c1

InChI

1S/C20H28N2.2ClH/c1-11-7-13(3)17(14(4)8-11)19(21)20(22)18-15(5)9-12(2)10-16(18)6;;/h7-10,19-20H,21-22H2,1-6H3;2*1H/t19-,20-;;/m0../s1

InChI 密鑰

HSFKFAWYBTVLDG-TULUPMBKSA-N

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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相关内容

The Chin group is interested in computational and experimental approaches to understanding stereoselective recognition and catalysis. Their studies in weak forces (H-bonding, electronic and steric effects) has led to a highly efficient method for making limitless varieties of chiral vicinal diamines from the 'mother diamine' that are useful for developing stereoselective organocatalysts or transition metal-based catalysts as well as for developing drugs (Acc Chem Res (2012) p1345). The 'mother diamine' is also useful for making binol, monophos and binap analogs. The Chin group is also interested in using reversible covalent bonds for stereoselective recognition and L to D conversion of natural and non-natural amino acids (EJOC (2012) p229).

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