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Merck

270016

Sigma-Aldrich

(±)-反式-1,2-二氨基环己烷

99%

别名:

(±)-反式-1,2-环己二胺

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About This Item

线性分子式:
C6H10(NH2)2
CAS号:
分子量:
114.19
Beilstein:
3193807
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽壓力

0.4 mmHg ( 20 °C)

化驗

99%

形狀

liquid

折射率

n20/D 1.489 (lit.)

bp

79-81 °C/15 mmHg (lit.)

mp

14-15 °C (lit.)

密度

0.951 g/mL at 25 °C (lit.)

SMILES 字串

N[C@@H]1CCCC[C@H]1N

InChI

1S/C6H14N2/c7-5-3-1-2-4-6(5)8/h5-6H,1-4,7-8H2/t5-,6-/m1/s1

InChI 密鑰

SSJXIUAHEKJCMH-PHDIDXHHSA-N

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一般說明

(±)-反式-1,2-二氨基环己烷被广泛用作配位化学和有机催化中的配体。它也充当不对称催化中的非手性配体。(±)-反式-1,2-二氨基环己烷可与脂肪族二醛缩合形成[3+3]或[2+2]大环化产物

應用

(±)-反式-1,2-二氨基环己烷可用于合成大环[3+3]六席夫碱。它也可用于多齿配体、手性助剂 和手性固定相的合成。

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

156.2 °F - closed cup

閃點(°C)

69 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Marcin Kwit et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(31), 8688-8695 (2007-07-31)
Aliphatic dialdehydes of rigid structures having a cyclohexane, a bicyclo[2.2.2]octane or a [7]triangulane skeleton, have been condensed with enantiomerically pure trans-1,2-diaminocyclohexane to give [3+3] or [2+2] macrocyclization products. Unlike acyclic aliphatic imines, these macrocyclic oligoimines show enhanced stabilities and their
Jana Hodacová et al.
Organic letters, 9(26), 5641-5643 (2007-11-22)
2,2'-Bipyridine-5,5'-dicarbaldehyde has been prepared in two steps by enamination of 5,5'-dimethyl-2,2'-bipyridine with Bredereck's reagent, and subsequent oxidative cleavage of the enamine groups with sodium periodate. On condensation of this dialdehyde with enantiomerically pure trans-1,2-diaminocyclohexane, the macrocyclic [3+3] hexa Schiff base
Enantiopure Monoprotected cis-1, 2-Diaminocyclohexane: One-Step Preparation and Application in Asymmetric Organocatalysis
A Berkessel, et al
ChemCatChem, 2, 1215-1218 (2010)
Tetrahedron, 49, 4419-4419 (1993)
trans-1, 2-Diaminocyclohexane derivatives as chiral reagents, scaffolds, and ligands for catalysis: applications in asymmetric synthesis and molecular recognition
YL Bennani, et al.
Chemical Reviews, 97, 3161-3196 null

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