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About This Item
Empirical Formula (Hill Notation):
C9H16N2
Molecular Weight:
152.24
UNSPSC Code:
12352302
PubChem Substance ID:
MDL number:
Concentration:
1 M in THF
Form:
liquid
form
liquid
concentration
1 M in THF
refractive index
n20/D 1.425
density
0.899 g/mL at 25 °C
SMILES string
C1CCN2CCCN=C2CC1
InChI
1S/C9H16N2/c1-2-5-9-10-6-4-8-11(9)7-3-1/h1-8H2
InChI key
GQHTUMJGOHRCHB-UHFFFAOYSA-N
signalword
Danger
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
-0.0 °F
flash_point_c
-17.8 °C
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system, Respiratory system
Regulatory Information
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Naoto Utsumi et al.
Organic letters, 10(16), 3405-3408 (2008-07-18)
Direct organocatalytic Mannich-type reactions of thioesters provide for the expedient and diastereoselective synthesis of protected beta-amino acids. A variety of thioesters were found to be reactive with different imines under mild conditions to provide beta-amino acids in good yields. This
Matthew O'Reilly et al.
Dalton transactions (Cambridge, England : 2003), (31)(31), 6092-6095 (2010-05-08)
With the new chiral phosphine ligand DBUP, obtained from DBU and Ph(2)PCl, a remarkable anion effect was observed on the diastereoselective formation of the bischelated complexes [Ni(DBUP)(2)](X)(n) (X = Cl, Br, n = 2; X = NiCl(4), n = 1)
Ning Zhu et al.
Journal of combinatorial chemistry, 12(4), 531-540 (2010-06-01)
The thiol-disulfide dynamic interchange reaction mediated by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) was extensively studied. By this synthetic method sulfides can be prepared successfully within seconds in high yields at room temperature from stable and readily available disulfides and an alkylating agent. The



