Conditions | Yield |
---|---|
With thionyl chloride Reflux; | 100% |
With thionyl chloride In N,N-dimethyl-formamide for 3h; Reflux; | 97% |
With thionyl chloride; N,N-dimethyl-formamide for 3h; Reflux; | 97% |
hexadecanoic acid methyl ester
A
methylene chloride
B
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
With tungsten(VI) chloride In benzene at 20℃; for 90h; Product distribution; |
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; |
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide In dichloromethane at 20℃; for 1h; | |
In dichloromethane for 12h; Inert atmosphere; |
DL-3,4,5,6-Tetra-O-benzyl-3,5/4,6-tetrahydroxycyclohex-1-ene-1-methanol
n-hexadecanoyl chloride
methyl Hexadecanoate
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 2h; Ambient temperature; | 100% |
9-{[(1,3-dihydroxypropan-2-yl)oxy]methyl}-2-{[(4-methoxyphenyl)diphenylmethyl]amino}-6,9-dihydro-1H-purin-6-one
n-hexadecanoyl chloride
Hexadecanoic acid 3-hexadecanoyloxy-2-(2-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-6-oxo-1,6-dihydro-purin-9-ylmethoxy)-propyl ester
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 20h; Ambient temperature; | 100% |
1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-2-hydroxymethyl-3-propanol
n-hexadecanoyl chloride
Hexadecanoic acid 2-hexadecanoyloxymethyl-3-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-propyl ester
Conditions | Yield |
---|---|
With dmap In pyridine for 2h; Heating; | 100% |
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
With potassium carbonate In water; ethyl acetate for 2h; Ambient temperature; | 100% |
N-octyl-2,3:4,6-di-O-isopropylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine
n-hexadecanoyl chloride
Hexadecanoic acid octyl-((3aS,4R,9aR,9bS)-2,2,8,8-tetramethyl-4,6,9a,9b-tetrahydro-3aH-[1,3]dioxolo[4',5':3,4]benzo[1,2-d][1,3]dioxin-4-yl)-amide
Conditions | Yield |
---|---|
In pyridine for 1h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
With pyridine at 20℃; for 3h; Acylation; | 4.5 g |
With triethylamine In dichloromethane at 20℃; for 4h; Inert atmosphere; |
(+)-1-O-[12-N-(benzyloxycarbonyl)aminododecanoyl]-3-O-(4-methoxybenzyl)-sn-glycerol
n-hexadecanoyl chloride
(+)-1-O-[12-N-(benzyloxycarbonyl)aminododecanoyl]-2-O-hexadecanoyl-3-O-(4-methoxybenzyl)-sn-glycerol
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane at 0 - 20℃; | 100% |
With pyridine; dmap In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
With pyridine; dmap In dichloromethane | 90% |
Stage #1: (+)-1-O-[12-N-(benzyloxycarbonyl)aminododecanoyl]-3-O-(4-methoxybenzyl)-sn-glycerol With pyridine; dmap In dichloromethane at 0℃; for 0.5h; Stage #2: n-hexadecanoyl chloride In dichloromethane at 20℃; Further stages.; | 70% |
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
With dmap In pyridine at 20℃; for 20h; | 100% |
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
Stage #1: 3-[4-(3α-hydroxynortropanylazo)phenoxy]propyloxymethylpolystyrene; n-hexadecanoyl chloride With dmap; triethylamine In dichloromethane at 20℃; for 12h; Stage #2: With trifluoroacetic acid In dichloromethane at 0℃; Further stages.; | 100% |
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
Stage #1: 3-[3-(4-hydroxypiperidinylazo)phenoxy]propyloxymethylpolystyrene; n-hexadecanoyl chloride With dmap; triethylamine In dichloromethane at 20℃; for 12h; Stage #2: With trifluoroacetic acid In dichloromethane at 0℃; Further stages.; | 100% |
Conditions | Yield |
---|---|
In methanol; sodium hydroxide; dichloromethane; chloroform | 100% |
2-(2-Aminoethoxy)ethanol
n-hexadecanoyl chloride
N-(ω-hydroxyethoxyethyl)hexadecanamide
Conditions | Yield |
---|---|
Stage #1: 2-(2-Aminoethoxy)ethanol With magnesium oxide In tetrahydrofuran; water at 5℃; for 0.5h; Stage #2: n-hexadecanoyl chloride In tetrahydrofuran; water at 5 - 10℃; for 2h; | 100% |
With triethylamine In dichloromethane at 0℃; for 4h; | 92% |
With magnesium oxide In tetrahydrofuran; water |
1-hydroxy-pyrrolidine-2,5-dione
n-hexadecanoyl chloride
palmitic acid N-succinimide ester
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; for 8h; Cooling with ice; | 100% |
With triethylamine In chloroform at 20℃; for 8h; Cooling with ice; | 100% |
Conditions | Yield |
---|---|
Stage #1: 2-amino-5,10,15,20-tetraphenylporphyrin With triethylamine In dichloromethane at 20℃; for 0.25h; Stage #2: n-hexadecanoyl chloride In dichloromethane at 20℃; for 3h; | 100% |
(3R)-3-hydroxytetradecanoic acid phenacyl ester
n-hexadecanoyl chloride
Hexadecanoic acid (R)-1-(2-oxo-2-phenyl-ethoxycarbonylmethyl)-dodecyl ester
Conditions | Yield |
---|---|
With dmap In pyridine; dichloromethane Ambient temperature; | 99.4% |
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 12h; | 99% |
In dichloromethane; water at 20℃; for 24h; | 92% |
With water |
n-hexadecanoyl chloride
pentadecanyl isocyanate
Conditions | Yield |
---|---|
With sodium azide In para-xylene for 2h; Heating; | 99% |
With sodium azide; benzene | |
With sodium azide In toluene for 5h; Reflux; Inert atmosphere; |
thiazolidine-2-thione
n-hexadecanoyl chloride
1-(2-Thioxo-thiazolidin-3-yl)-hexadecan-1-one
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 50℃; for 0.5h; | 99% |
With triethylamine In dichloromethane at 0 - 5℃; for 3h; | 75% |
N-hydroxy-N-methylbenzenecarbothioamide
n-hexadecanoyl chloride
N-methyl-N-palmitoyloxythiobenzamide
Conditions | Yield |
---|---|
With pyridine In diethyl ether for 0.5h; Ambient temperature; | 99% |
DL-(1,2,4/3,5,6)-2,5,6-Tri-O-benzyl-2,3,4,5,6-pentahydroxy-3,4-bis-O-(4-methoxybenzyl)cyclohexane-1-methanol, DL-(1,2,3,5/4,6)-2,3,6-Tri-O-benzyl-2,3,4,5,6-pentahydroxy-4,5-bis-O-(4-methoxybenzyl)cyclohexane-1-methanol
n-hexadecanoyl chloride
methyl Hexadecanoate, methyl Hexadecanoate
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane at 25℃; for 1h; | 99% |
rac-1-O-hexadecyl-3-O-benzylglycerol
n-hexadecanoyl chloride
Hexadecanoic acid 2-benzyloxy-1-hexadecyloxymethyl-ethyl ester
Conditions | Yield |
---|---|
With pyridine In benzene at 70℃; | 99% |
Conditions | Yield |
---|---|
In toluene at 35℃; for 1h; | 99% |
With pyridine In 1,2-dichloro-ethane |
6,7dihydroxy-3methyl-4-thiaheptanoic acid t-butyl ester
n-hexadecanoyl chloride
6,7-bis(palmitoyloxy)-3-methyl-4-thiaheptanoic acid t-butyl ester
Conditions | Yield |
---|---|
With dmap In dichloromethane for 1h; Ambient temperature; | 99% |
With 2-(Dimethylamino)pyridine; sodium bicarbonate; triethylamine; citric acid In chloroform; water | 99% |
(S)-2-(4-{[3-(3-Hexadecanoylamino-2-hydroxy-propylsulfanyl)-propionylamino]-methyl}-benzoylamino)-pentanedioic acid di-tert-butyl ester
n-hexadecanoyl chloride
(S)-2-(4-{[3-(3-Hexadecanoylamino-2-hexadecanoyloxy-propylsulfanyl)-propionylamino]-methyl}-benzoylamino)-pentanedioic acid di-tert-butyl ester
Conditions | Yield |
---|---|
With dmap In dichloromethane for 0.5h; Ambient temperature; | 99% |
methyl furan-2-ylacetate
n-hexadecanoyl chloride
(5-hexadecanoylfuran-2-yl)acetic acid methyl ester
Conditions | Yield |
---|---|
With tin(IV) chloride In dichloromethane at -5℃; for 1h; | 99% |
With tin(IV) chloride In dichloromethane at -5℃; for 1h; Friedel-Crafts acylation; | 98% |
With tin(IV) chloride In dichloromethane at -5℃; for 1h; Substitution; Friedel-Crafts reaction; | |
With tin(IV) chloride In dichloromethane at -5℃; Friedel-Crafts acylation; |
3-O-Benzyl-1-O-octadecanoyl-sn-glycerin
n-hexadecanoyl chloride
3-O-benzyl-2-O-hexadecanoyl-1-O-octadecanoyl-sn-glycerol
Conditions | Yield |
---|---|
With dmap In pyridine; dichloromethane at 0 - 20℃; Acylation; | 99% |
(S)-3-Hydroxy-2-(2-tetradecanoylamino-acetylamino)-propionic acid benzyl ester
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; for 6h; Acylation; | 99% |
O-(5-Acetamido-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonic acid)-(2->3)-O-β-D-galactopyranosyl)-(1->4)-O-β-D-glucopyranosyl)-(1->1)-(2S,3R,4E)-2-amino-4-octadecene-1,3-diol
n-hexadecanoyl chloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran at 20℃; for 2h; | 99% |
With sodium acetate In tetrahydrofuran; water Acylation; |
glycine ethyl ester hydrochloride
n-hexadecanoyl chloride
N-hexadecanoyl glycine methyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 99% |
With sodium hydrogencarbonate In chloroform; water at 20℃; for 2h; | |
Stage #1: glycine ethyl ester hydrochloride With potassium carbonate In dichloromethane; water at 0℃; for 0.0833333h; Stage #2: n-hexadecanoyl chloride In dichloromethane; water at 20℃; for 16h; | 1.48 g |
IUPAC Name: Hexadecanoyl chloride
Synonyms of Palmitoyl chloride (CAS NO.112-67-4): AI3-52614 ; EINECS 203-996-7 ; HSDB 5573 ; Hexadecanoic acid, chloride ; NSC 9854 ; Palmitic acid chloride ; Palmityl chloride ; Hexadecanoyl chloride
CAS NO: 112-67-4
Molecular Formula of Palmitoyl chloride (CAS NO.112-67-4): C16H31ClO
Molecular Weight: 274.8697
Molecular Structure:
Melting Point: 11-13 °C
ProductCategories: ACID CHLORIDES
Polar Surface Area: 17.07 Å2
Index of Refraction: 1.45
Molar Refractivity: 81.05 cm3
Molar Volume: 301.1 cm3
Surface Tension: 31.2 dyne/cm
Density of Palmitoyl chloride (CAS NO.112-67-4): 0.912 g/cm3
Flash Point: 155.5 °C
Enthalpy of Vaporization: 56.54 kJ/mol
Boiling Point: 323.5 °C at 760 mmHg
Vapour Pressure: 0.000261 mmHg at 25°C
Palmitoyl chloride (CAS NO.112-67-4) is used as intermediates in organic synthesis.
Hazard Codes: C
Risk Statements: 14-34-29
R14: Reacts violently with water.
R34: Causes burns.
R29: Contact with water liberates toxic gas.
Safety Statements: 26-36/37/39-43-45-8
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
S43: In case of fire use ... (there follows the type of fire-fighting equipment to be used.)
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S8: Keep container dry.
RIDADR: UN 3265 8/PG 2
WGK Germany: 1
F: 9-21
HazardClass: 8
PackingGrou:p II
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