Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide at -5 - 70℃; for 4.33333h; | 98.1% |
With thionyl chloride; N,N-dimethyl-formamide at 20℃; for 24h; | 95% |
With thionyl chloride In chloroform at 65℃; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 1h; Ambient temperature; | 100% |
With triethylamine In tetrahydrofuran at 0℃; for 1h; | 100% |
In 1,4-dioxane; pyridine for 2h; Ambient temperature; | 83% |
With iodine; magnesium; benzene |
Conditions | Yield |
---|---|
With triethylamine In benzene at 10 - 20℃; | 100% |
With triethylamine In benzene at 10 - 20℃; | 100% |
With triethylamine In tetrahydrofuran at 0 - 20℃; for 20h; | 99% |
With potassium carbonate In diethyl ether | 82% |
Conditions | Yield |
---|---|
With pyridine In chloroform for 1h; | 100% |
tetradecanoyl chloride
N-octyl-2,3:4,6-di-O-isopropylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine
Tetradecanoic 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% |
1-O-allyl-3,4,5,6-tetra-O-benzyl-D-myo-inositol
tetradecanoyl chloride
Conditions | Yield |
---|---|
With pyridine | 100% |
tetradecanoyl chloride
(R)-5-[(tert-butyldimethylsilyloxy)methyl]-5-(hydroxymethyl)tetrahydro-2-furanone
(R)-5-[(tert-butyldimethylsilyloxy)methyl]-5-[(tetradecanoyloxy)methyl]tetrahydro-2-furanone
Conditions | Yield |
---|---|
With pyridine at 20℃; | 100% |
Conditions | Yield |
---|---|
With pyridine at 20℃; for 12h; | 100% |
With pyridine for 12h; | 99% |
tetradecanoyl chloride
4-hydroxy-6-methoxy-(2H)-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With pyridine at 20℃; for 12h; | 100% |
3,4-dibromothiophene
tetradecanoyl chloride
(3,4-dibromothien-2-yl)-tridecyl-ketone
Conditions | Yield |
---|---|
aluminum (III) chloride In dichloromethane at 0℃; Friedel Crafts Acylation; Inert atmosphere; | 100% |
Stage #1: 3,4-dibromothiophene; tetradecanoyl chloride With aluminum (III) chloride In dichloromethane at 0℃; Inert atmosphere; Stage #2: With hydrogenchloride In dichloromethane; water |
L-glutamic acid α-tert-butyl ester
tetradecanoyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 24h; Sealed tube; Inert atmosphere; | 100% |
(3-(5H,6H-11,12-didehydrodibenzo[b,f]azocin-5-yl)-3-oxopropyl)amine
tetradecanoyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 1h; | 100% |
tetradecanoyl chloride
(±)-4-hydroxymethyl-4-vinyl-dihydro-furan-2-one
4-<(tetradecanoyloxy)methyl>-4-vinyltetrahydro-2-furanone
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 2h; Ambient temperature; | 99% |
With pyridine; 2-(Dimethylamino)pyridine In dichloromethane; ethyl acetate | 99% |
tetradecanoyl chloride
Conditions | Yield |
---|---|
With potassium hydroxide | 99% |
1,3-cylohexanedione
tetradecanoyl chloride
Tetradecanoic acid 3-oxo-cyclohex-1-enyl ester
Conditions | Yield |
---|---|
With pyridine In chloroform for 1h; | 98% |
Conditions | Yield |
---|---|
Stage #1: 5-hydroxynaphtho-1,4-quinone With triethylamine In diethyl ether at 20℃; for 0.5h; Stage #2: tetradecanoyl chloride In diethyl ether at 20℃; for 1h; | 98% |
With triethylamine In benzene Heating; | |
With dmap In dichloromethane at 0 - 20℃; |
tetradecanoyl chloride
(R)-5-((S)-2-Benzyloxy-1-hydroxy-ethyl)-dihydro-furan-2-one
Tetradecanoic acid (S)-2-benzyloxy-1-((R)-5-oxo-tetrahydro-furan-2-yl)-ethyl ester
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 3h; Ambient temperature; | 98% |
tetradecanoyl chloride
1,5-anhydro-4,6-O-benzylidene-2-deoxy-2-C-(2-propenyl)-D-glucitol
1,5-anhydro-4,6-O-benzylidene-2-deoxy-2-C-(2-propenyl)-3-O-myristoyl-D-glucitol
Conditions | Yield |
---|---|
With pyridine at 20℃; for 3h; | 98% |
7-triethylsilyl-10-deacetylbaccatin III
tetradecanoyl chloride
7-triethylsilyl-10-tetradecanoyl-10-deacetylbaccatin III
Conditions | Yield |
---|---|
With lithium hexamethyldisilazane In tetrahydrofuran at -40 - 0℃; Schotten-Baumann reaction; | 98% |
Conditions | Yield |
---|---|
Stage #1: 5-hydroxy-2-methyl-1,4-naphthoquinone With triethylamine In diethyl ether at 20℃; for 0.5h; Stage #2: tetradecanoyl chloride In diethyl ether at 20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 98% |
7-ethyl-10-hydroxycamptothecin
tetradecanoyl chloride
Conditions | Yield |
---|---|
Stage #1: 7-ethyl-10-hydroxycamptothecin With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane; N,N-dimethyl acetamide for 0.333333h; Cooling with ice; Stage #2: tetradecanoyl chloride In dichloromethane; N,N-dimethyl acetamide at 20℃; for 12h; Reagent/catalyst; Solvent; Cooling with ice; | 97.98% |
azetidine-3-ol
tetradecanoyl chloride
Conditions | Yield |
---|---|
With triethylamine In methanol | 97% |
serine ethyl ester hydrochloride
tetradecanoyl chloride
D,L-Serine O-myristoyl ethyl ester hydrochloride
Conditions | Yield |
---|---|
at 40℃; for 5h; | 97% |
(5S)-5-(hydroxymethyl)-5H-furan-2-one
tetradecanoyl chloride
5-O-tetradecanoyl-2,3-didehydro-2,3-dideoxy-D-glycero-pentono-1,4-lactone
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 24h; Ambient temperature; | 97% |
5-O-(tert-butyldiphenylsilyl)-2-deoxy-L-ribonolactone
tetradecanoyl chloride
5-O-(tert-butyldiphenylsilyl)-3-O-tetradecanoyl-2-deoxy-L-ribonolactone
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 20h; Ambient temperature; | 97% |
tetradecanoyl chloride
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane 1.) 0 deg C, 1 h, 2.) RT, 15 h; | 97% |
tetradecanoyl chloride
(5S)-5-[(1S)-2-benzyloxy-1-hydroxyethyl]tetrahydrofuran-2-one
Tetradecanoic acid (S)-2-benzyloxy-1-((S)-5-oxo-tetrahydro-furan-2-yl)-ethyl ester
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 3h; Ambient temperature; | 97% |
tetradecanoyl chloride
Propargylamine
N-(prop-2-yn-1-yl)tetradecanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 1h; | 97% |
di(pyridin-2-yl)amine
tetradecanoyl chloride
N,N-di(pyridin-2-yl)tetradecanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; Inert atmosphere; | 97% |
Molecular Structure of Myristoyl chloride (112-64-1):
EINECS: 203-994-6
IUPAC Name: Tetradecanoyl chloride
Molecular Formula: C14H27ClO
Molecular Weight: 246.816580 g/mol
XLogP3: 6.3
H-Bond Donor: 0
H-Bond Acceptor: 1
Index of Refraction: 1.448
Molar Refractivity: 71.78 cm3
Molar Volume: 268.1 cm3
Surface Tension: 30.9 dyne/cm
Density: 0.92 g/cm3
Flash Point: 139.6 °C
Melting Point: -1 °C
Boiling Point: 296.5 °C at 760 mmHg
Enthalpy of Vaporization: 53.63 kJ/mol
Vapour Pressure: 0.00143 mmHg at 25 °C
Water Solubility: 0.5779 mg/L at 25 °C
Refractive Index: n20/D 1.449(lit.)
Storage temp.: -20°C
Canonical SMILES: CCCCCCCCCCCCCC(=O)Cl
InChI: InChI=1S/C14H27ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3
InChIKey: LPWCRLGKYWVLHQ-UHFFFAOYSA-N
Ecotoxicity Information of Myristoyl chloride (112-64-1):
Fish: Leuciscus idus: LC50 > 1000 mg/l; 96H; acuut
Bacteria: EC10 > 10000 mg/l; 16H;
Safety Information of Myristoyl chloride (112-64-1):
Hazard Codes: C
Risk Statements: 34-37-22
34: Causes burns
37: Irritating to the respiratory system
22: Harmful if swallowed
Safety Statements: 26-36/37/39-45-28B
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39: Wear suitable protective clothing, gloves and eye/face protection
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
28: After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer)
RIDADR: UN 3265 8/PG 2
WGK Germany: 3
HazardClass: 8
PackingGroup: III
F: 10-21
Myristoyl chloride (112-64-1) is a kind of acid chlorides with appearance of clear colorless to light yellowish-brown liquid. It is also called for n-Tetradecanoyl chloride ; Tetradecanoyl chloride ; Myristoyl chloride 99+% ; Myristoyl chloride 98% ; Myristoyl chloride 98+% .
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