669660
(S,S)-(+)-N,N′-Dimethyl-1,2-cyclohexanediamine
≥97.0% (GC)
Synonym(s):
(1S)-trans-1,2-Bis(methylamino)cyclohexane, (S,S)-N,N′-Dimethyl-1,2-diaminocyclohexane
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About This Item
Empirical Formula (Hill Notation):
C8H18N2
CAS Number:
Molecular Weight:
142.24
Beilstein:
4304824
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Assay
≥97.0% (GC)
optical activity
[α]/D +145±5°, c = 4.47 in chloroform
mp
39-44 °C
functional group
amine
storage temp.
2-8°C
SMILES string
CN[C@H]1CCCC[C@@H]1NC
InChI
1S/C8H18N2/c1-9-7-5-3-4-6-8(7)10-2/h7-10H,3-6H2,1-2H3/t7-,8-/m0/s1
InChI key
JRHPOFJADXHYBR-YUMQZZPRSA-N
Application
(S,S)-(+)-N,N′-Dimethyl-1,2-cyclohexanediamine can be used:
- To synthesize derivatives of α-diazophosphonic acid, which are employed in O-H and N-H insertion reactions.
- As a starting material for the synthesis of α-chloro-α-alkylphosphonic acids.
- To prepare C2 symmetrical diamine enantiomers of C60 with chirospectrosopic properties.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
165.2 °F - closed cup
Flash Point(C)
74 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and characterization of both enantiomers of a chiral C60 derivative with C2 symmetry
Maggini M, et al.
Tetrahedron Letters, 36(16), 2845-2846 (1995)
Preparation of chiral α-diazophosphonic acid derivatives
Moody CJ, et al.
Tetrahedron Asymmetry, 12(11), 1657-1661 (2001)
(3a R, 7a R)-2-Ethyloctahydro-1 H-1, 3-dineopentyl-1, 3, 2-benzodiazaphosphole Oxide
Encyclopedia of Reagents for Organic Synthesis, Second Edition, 12(11), 1657-1661 (2001)
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