lauric acid
L-lysine
A
N-lauroyl-L-lysine
B
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With Streptomyces mobaraensis NBRC 13819 acylase In glycerol at 37℃; for 48h; pH=7.5; | A 5% B 44% |
Conditions | Yield |
---|---|
at 80℃; for 54h; Inert atmosphere; | A 32% B 23% |
Conditions | Yield |
---|---|
With hydrogenchloride at 20℃; | 96% |
n-dodecanoyl chloride
Nε-lauroyl-L-lysine
Nα,Nε-bis(1-oxododecyl)-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 96% |
With sodium hydroxide In diethyl ether at 0 - 20℃; |
suberoyl chloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 96% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 82% |
isononanoyl chloride
Nε-lauroyl-L-lysine
Nε-(1-oxododecyl)-Nα-(3,5,5-trimethyl-1-oxohexyl)-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 94% |
With sodium hydroxide In diethyl ether at 0 - 20℃; |
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 94% |
With sodium hydroxide In diethyl ether at 0 - 20℃; |
Conditions | Yield |
---|---|
Stage #1: 1-Decanol; Nε-lauroyl-L-lysine With toluene-4-sulfonic acid In benzene at 130℃; for 48h; Stage #2: With morpholine In methanol Further stages.; | 93% |
With toluene-4-sulfonic acid for 48h; Heating; | 91% |
gloutaric dichloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 93% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 79% |
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 93% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 83% |
Conditions | Yield |
---|---|
With hydrogenchloride at 20℃; | 93% |
Nε-lauroyl-L-lysine
cyclohexanylcarbonyl chloride
Nα-(cyclohexylcarbonyl)-Nε-(1-oxododecyl)-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 92% |
With sodium hydroxide In diethyl ether at 0 - 20℃; |
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 92% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 82% |
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 92% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 82% |
isononanol
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
90% |
Adipic acid dichloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 90% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 80% |
1-dodecyl alcohol
Nε-lauroyl-L-lysine
Nε-lauroyl-L-lysine dodecyl ester
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 48h; Heating; | 89% |
succinoyl dichloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 88% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 68% |
Hexanoyl chloride
Nε-lauroyl-L-lysine
Nα-hexanoyl-Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 88% |
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 85% |
Nε-lauroyl-L-lysine
2-ethylhexanoic acid chloride
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 86% |
With sodium hydroxide In diethyl ether at 0 - 20℃; |
11-bromoundecanoyl chloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; under 24 Torr; | 85% |
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h; | 85% |
1-Bromo-11-hydroxyundecane
Nε-lauroyl-L-lysine
Nε-lauroyl-L-lysine 11-bromoundecyl ester
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene at 130℃; for 48h; | 80% |
1,12-dodecanedioyl dichloride
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 80% |
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 20℃; for 23h; | 79% |
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 65% |
Nε-lauroyl-L-lysine
malonoyl dichloride
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h; | 70% |
ethyl 6-chloro-6-oxohexanoate
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
With water; sodium hydroxide at 20℃; for 24h; | 66% |
Conditions | Yield |
---|---|
With hydrogenchloride at 0 - 20℃; |
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 85 percent / aq. NaOH / diethyl ether / 0 - 20 °C / 24 Torr 2: 98 percent / 24 h / 100 °C View Scheme | |
Multi-step reaction with 2 steps 1: 85 percent / NaOH / H2O; diethyl ether / 24 h / 0 - 20 °C 2: 98 percent / 24 h / 100 °C View Scheme |
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 93 percent / HCl / 20 °C 2: 91 percent / Et3N / tetrahydrofuran / 24 h / 20 °C View Scheme |
Nε-lauroyl-L-lysine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 93 percent / Et3N / tetrahydrofuran / 24 h / 20 °C View Scheme |
The N'-Laruoyl-L-lysine with the cas number 52315-75-0 is also called N6-(1-Oxododecyl)-L-lysine. The IUPAC name is (2S)-2-amino-6-(dodecanoylamino)hexanoic acid. Its EINECS registry number is 257-843-4. The molecular formula of this chemical is C18H36N2O3. This chemical is a kind of organics. It should be stored in dry and cool environment.
The properties of the chemical are: (1)ACD/LogP: 3.89; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.39; (4)ACD/LogD (pH 7.4): 1.39; (5)ACD/BCF (pH 5.5): 1.69; (6)ACD/BCF (pH 7.4): 1.68; (7)ACD/KOC (pH 5.5): 9.86; (8)ACD/KOC (pH 7.4): 9.83; (9)#H bond acceptors: 5; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 17; (12)Polar Surface Area: 49.85Å2; (13)Index of Refraction: 1.481; (14)Molar Refractivity: 94.12 cm3; (15)Molar Volume: 330.2 cm3; (16)Polarizability: 37.31×10-24cm3; (17)Surface Tension: 39.7 dyne/cm; (18)Enthalpy of Vaporization: 87.81 kJ/mol; (19)Vapour Pressure: 1.48×10-12 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: O=C(NCCCC[C@H](N)C(=O)O)CCCCCCCCCCC
(2)InChI: InChI=1/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1
(3)InChIKey: GYDYJUYZBRGMCC-INIZCTEOBA
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