As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryMYRISTOLEIC ACID CAS:544-64-9 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermedia
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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inquiryConditions | Yield |
---|---|
With sodium hydroxide In water; acetone for 14h; Heating; | A 80% B 50% |
myristoleic acid ethyl ester
myristoleic acid
Conditions | Yield |
---|---|
With sodium hydroxide | |
With sodium hydroxide In methanol | |
With water; sodium hydroxide at 20℃; for 3h; |
9-tetradecynoic acid
myristoleic acid
Conditions | Yield |
---|---|
With quinoline; hydrogen; palladium on barium sulfate In methanol |
(Z)-9-tetradecen-1-ol
myristoleic acid
Conditions | Yield |
---|---|
With dipyridinium dichromate In N,N-dimethyl-formamide at 25℃; for 12h; Oxidation; |
8-bromooctanoic acid
myristoleic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) LiNH2, liq. NH3, (ii) /BRN= 1756103/, THF 2: H2, quinoline / Pd-BaSO4 / methanol View Scheme | |
Multi-step reaction with 5 steps 1: acetyl chloride / 4 h / 20 °C 2: 18 h / 20 °C 3: sodium phosphinate / 2 h / 40 °C 4: sodium hexamethyldisilazane / tetrahydrofuran / 2 h / -78 - 20 °C 5: sodium hydroxide; water / 3 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) LiNH2, liq. NH3, (ii) /BRN= 1756103/, THF 2: H2, quinoline / Pd-BaSO4 / methanol View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (i) O3, CH2Cl2, (ii) Ph3P 2: (i) K, HMPT, (ii) /BRN= 1769505/ 3: aq. NaOH / methanol View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) K, HMPT, (ii) /BRN= 1769505/ 2: aq. NaOH / methanol View Scheme | |
Multi-step reaction with 2 steps 1: sodium hexamethyldisilazane / tetrahydrofuran / 2 h / -78 - 20 °C 2: sodium hydroxide; water / 3 h / 20 °C View Scheme |
myristoleic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium phosphinate / 2 h / 40 °C 2: sodium hexamethyldisilazane / tetrahydrofuran / 2 h / -78 - 20 °C 3: sodium hydroxide; water / 3 h / 20 °C View Scheme |
Ethyl 8-bromooctanoate
myristoleic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 18 h / 20 °C 2: sodium phosphinate / 2 h / 40 °C 3: sodium hexamethyldisilazane / tetrahydrofuran / 2 h / -78 - 20 °C 4: sodium hydroxide; water / 3 h / 20 °C View Scheme |
myristoleic acid
10-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With recombinant Chryseobacterium gleum oleate hydratase In aq. phosphate buffer at 25℃; for 21h; pH=6.5; Catalytic behavior; Reagent/catalyst; | 95% |
With oleate hydratase from macrococcus caseolyticus; water; flavin adenine dinucleotide In ethanol at 25℃; for 0.166667h; pH=6.5; PIPES buffer; Enzymatic reaction; |
myristoleic acid
di-tert-butyl butane-1,4-diylbis((3-aminopropyl)carbamate)
N1,N12-dimyristoleoyl-N4,N9-di(t-butoxycarbonyl)-1,12-diamino-4,9-diazadodecane
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 16h; | 76% |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: glycine ethyl ester hydrochloride With triethylamine In N,N-dimethyl-formamide for 18h; | 70% |
myristoleic acid
3-O-[2,3,4-tri-O-(tert-butyldimethylsilyl)-6-deoxy-6-thioacetyl-α-D-glucopyranosyl]-glycerol
3-O-[2,3,4-tri-O-(tert-butyldimethylsilyl)-6-deoxy-6-thioacetyl-α-D-glucopyranosyl]-1-O-myristoleoyl-glycerol
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 6h; esterification; | 60.9% |
Conditions | Yield |
---|---|
Stage #1: diiodomethane With diethylzinc; 2,4,6-Trichlorophenol In hexane; dichloromethane at -40℃; for 0.25h; Inert atmosphere; Stage #2: myristoleic acid In hexane; dichloromethane at -40 - 20℃; Inert atmosphere; | 39% |
myristoleic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at -20 - 20℃; for 16h; Inert atmosphere; regioselective reaction; | 28% |
myristoleic acid
(+/-)-threo-9.10-dihydroxy-myristic acid
Conditions | Yield |
---|---|
With formic acid; dihydrogen peroxide at 40℃; for 2h; |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 4h; Heating; | 300 mg |
myristoleic acid
Conditions | Yield |
---|---|
With oxalyl dichloride for 3h; | |
With oxalyl dichloride In benzene at 20℃; for 2h; Inert atmosphere; |
myristoleic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide |
myristoleic acid
Conditions | Yield |
---|---|
Stage #1: (S)-2-{(S)-2-[(S)-2-((S)-2-{[(2S,4S)-1-(2-tert-Butoxycarbonylamino-2-methyl-propionyl)-4-hydroxy-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-4-carbamoyl-butyrylamino}-4-methyl-pentanoic acid methyl ester With trifluoroacetic acid at 20℃; for 0.333333h; Stage #2: myristoleic acid With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: 10-carbon-sphingosine In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2R,3S,4E)-2-aminododec-4-ene-1,3-diol In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: 15-carbon-sphingosine In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2S,3R,4E)-2-amino-4-octadecene-1,3-diol In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: 20-carbon-sphingosine In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2R,3S,4E)-2-aminooctadec-4-ene-1,3-diol In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2R,3R,4E)-2-amino-octadec-4-ene-1,3-diol In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2S,3S,4E)-L-threo sphingosine In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: dihydrosphingosine In tetrahydrofuran at 20℃; Further stages.; |
(+/-)-threo-dihydro-sphingosine
myristoleic acid
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (+/-)-threo-dihydro-sphingosine In tetrahydrofuran at 20℃; Further stages.; |
(2S,3R)-2-amino-1,3-octadecanediol
myristoleic acid
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (2S,3R)-2-amino-1,3-octadecanediol In tetrahydrofuran at 20℃; Further stages.; |
Conditions | Yield |
---|---|
Stage #1: myristoleic acid With dmap; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one at 20℃; Stage #2: (1S,2R)-(+)-norphedrine In tetrahydrofuran at 20℃; Further stages.; |
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