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inquiryProduct Name: Undecanedioic acid Synonyms: Undecanedioic acid UDDA;Nonane-1,9-dicarboxylic acid;Undecanedioic acid,97%;Undecanedioic acid,1,9-Nonanedicarboxylic acid;Nonamethylenedicarboxylic Acid Undecanedioic Acid;Undecane-1,11-dioic acid;Undeca
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inquiryWe are manufacturer of this product. If you are looking for the material's manufacturer or supplier in China, Ality Group is your best choice. Specifications of our Undecanedioic acidCAS 1852-04-6: Items
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inquiryCas No. 1852-04-6 Undecanedioic Acid (DC11) for cutting fluid Product Description Undecanedioic Acid Product Name: Undecanedioic Acid CAS#: 1852-04-6 M.F.:C11H20O4 M.W.:216.28 Appearance:White powder
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inquiryAbout Product Details Items Specifications Test Results Appearance White to white crystalline powde
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inquiryBeluga chemical professional supply High qualityUndecanedioic acid CAS 1852-04-6 1. Beluga Chemical has a professional RESEARCH and development team and strong technical force to ensure technical support and research capabilities. 2. Made in Chin
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Undecanedioic acid Basic information Description Product Name: Undecanedioic acid Synonyms: Undecanedioic acid UDDA;Nonane-1,9-dicarboxylic acid;Undecanedioic acid,97%;Nonamethylenedicarboxylic Acid Undecanedioic Acid;Undecanedioic acid,1,9-Non
factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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
Conditions | Yield |
---|---|
With chromium(VI) oxide; periodic acid In water; acetonitrile at 0 - 5℃; for 1.25h; | 90% |
With sodium bromate; hydrogen bromide; tert-butyl alcohol In tetrachloromethane; water for 2h; Ambient temperature; | 75% |
Oxydation; |
Methyl 11-nitroundecanoate
undecanedioic acid
Conditions | Yield |
---|---|
With hydrogenchloride In water for 4h; Nef reaction; Reflux; | 79% |
Conditions | Yield |
---|---|
With HeMaRaphos; water; toluene-4-sulfonic acid; palladium dichloride In tetrahydrofuran at 125℃; under 30003 Torr; for 24h; Autoclave; Green chemistry; regioselective reaction; | 63% |
Conditions | Yield |
---|---|
With porcine liver esterase; sodium hydroxide; phosphate buffer for 6h; | 49% |
Conditions | Yield |
---|---|
With recombinant escherichia coli BL21(DE3); Tween 84 In aq. buffer at 35℃; for 2h; pH=8; Enzymatic reaction; | 36% |
Conditions | Yield |
---|---|
With chromium(VI) oxide; acetic acid |
Conditions | Yield |
---|---|
With potassium permanganate; acetone | |
With ozone |
Conditions | Yield |
---|---|
With alkaline KMNO4 | |
With recombinant escherichia coli BL21(DE3); Tween 82 In aq. buffer at 35℃; for 2h; pH=8; Enzymatic reaction; |
Conditions | Yield |
---|---|
With nitric acid | |
With ammonium vanadate; nitric acid | |
With nitric acid |
methyl 12-hydroxyoctadecanoate
undecanedioic acid
Conditions | Yield |
---|---|
With ammonium vanadate; nitric acid; copper |
11-oxoundecanoic acid
undecanedioic acid
Conditions | Yield |
---|---|
With alkaline KMNO4 |
Conditions | Yield |
---|---|
With sodium hydroxide |
4-oxo-1,9-nonanedicarboxylic acid
undecanedioic acid
Conditions | Yield |
---|---|
With potassium hydroxide; hydrazine hydrate; diethylene glycol |
Conditions | Yield |
---|---|
With alkaline KMNO4 |
Conditions | Yield |
---|---|
With ammonium vanadate; nitric acid; copper |
triundecanoin
undecanedioic acid
Conditions | Yield |
---|---|
beim Abbau im menschlichen Organismus; |
1,11-undecanedinitrile
undecanedioic acid
Conditions | Yield |
---|---|
With potassium hydroxide durch Verseifen; | |
(alkaline hydrolysis); |
undec-5-ynedioic acid
undecanedioic acid
Conditions | Yield |
---|---|
With hydrogen; nickel | |
With hydrogen; platinum |
methyl 4-(2-oxo-1-cycloheptyl)butyrate
undecanedioic acid
Conditions | Yield |
---|---|
Multistep reaction; |
undecanedioic acid
Conditions | Yield |
---|---|
With potassium permanganate; sodium periodate |
undecanedioic acid
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol |
Conditions | Yield |
---|---|
With chromium(VI) oxide; sodium tetrahydroborate; sulfuric acid; water; tert-butyl alcohol 1.) THF, a.) r.t., 2 h, b.) 50-55 deg C, 4 h, 2.) acetone, r.t., 10 h; Yield given. Multistep reaction; | |
Multi-step reaction with 6 steps 1: methanol / 6 h / 0 - 20 °C 2: ozone; triphenylphosphine / methanol; dichloromethane / 6 h / -78 - 20 °C 3: sodium hydroxide / 1.5 h / 0 - 20 °C 4: methanesulfonyl chloride; triethylamine / dichloromethane / 0.17 h / 20 °C 5: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h / 20 °C / 2250.23 Torr 6: hydrogenchloride / water / 4 h / Reflux View Scheme |
cyclododecanol
A
azelaic acid
B
heptanedioic acid
C
octane-1,8-dioic acid
D
1,10-decanedioic acid
E
undecanedioic acid
F
1,12-dodecanedioic acid
Conditions | Yield |
---|---|
With nitric acid In Cyclopentane for 0.166667h; Product distribution; other temperature, other concentration of HNO3;; | A n/a B n/a C n/a D 0.020 (unit not given) E 0.110 (unit not given) F 0.824 (unit not given) |
cyclododecanol
A
1,10-decanedioic acid
B
undecanedioic acid
C
1,12-dodecanedioic acid
Conditions | Yield |
---|---|
With nitric acid at 50℃; for 0.166667h; Further byproducts given. Title compound not separated from byproducts; | A 0.021 (unit not given) B 0.110 (unit not given) C 0.824 |
cyclododecanone
A
1,5-pentanedioic acid
B
Adipic acid
C
1,10-decanedioic acid
D
succinic acid
E
undecanedioic acid
F
1,12-dodecanedioic acid
Conditions | Yield |
---|---|
With nitric acid for 0.75h; Product distribution; other temperature, other concentration of HNO3;; | A n/a B n/a C 0.030 (unit not given) D n/a E 0.117 (unit not given) F 0.742 (unit not given) |
cyclododecanone
A
1,10-decanedioic acid
B
undecanedioic acid
C
1,12-dodecanedioic acid
Conditions | Yield |
---|---|
With nitric acid at 45℃; for 0.166667h; Further byproducts given. Title compound not separated from byproducts; | A 0.030 (unit not given) B 0.117 (unit not given) C 0.742 |
A
lauric acid
B
1,10-decanedioic acid
C
undecylenic acid
D
undecanedioic acid
Conditions | Yield |
---|---|
With potassium permanganate In acetic acid Product distribution; |
A
11-oxoundecanoic acid
B
undecanedioic acid
Conditions | Yield |
---|---|
In benzene-d6 at 80℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
2-nitrocycloundecanone
undecanedioic acid
Conditions | Yield |
---|---|
With Oxone; sodium hydroxide; disodium hydrogenphosphate; water 1.) MeOH, 70 deg C, 4 h, 2.) MeOH, r.t., 4 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With thionyl chloride at 20℃; for 6h; | |
With thionyl chloride for 1.5h; Reflux; | 192.62 g |
undecanedioic acid
pentafluorophenyl trifloroacetate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1h; | 100% |
Conditions | Yield |
---|---|
With triphenylphosphine at 90℃; for 3h; | 99% |
With methoxyhydroquinone; triphenylphosphine at 90℃; for 3h; | 99% |
With triphenylphosphine at 90℃; for 3h; Concentration; | 99% |
undecanedioic acid
Conditions | Yield |
---|---|
With oxalyl dichloride; N,N-dimethyl-formamide In tetrahydrofuran at 25℃; for 2h; | 99% |
undecanedioic acid
undecanedioyl dichloride
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; | 95% |
With thionyl chloride | |
With thionyl chloride |
undecanedioic acid
1,11-undecanediamide
Conditions | Yield |
---|---|
With ammonia at 180 - 220℃; for 10h; Temperature; | 95% |
Multi-step reaction with 2 steps 1: thionyl chloride / 1.5 h / Reflux 2: ammonia / methanol / 1 h / 40 °C View Scheme |
undecanedioic acid
(2S,4R)-1-[(2S)-2-azanyl-3,3-dimethylbutanoyl]-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]-4-oxidanylpyrrolidine-2-carboxamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0℃; for 6h; | 78% |
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dimethyl sulfoxide at 0 - 20℃; | 76% |
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; for 12h; Inert atmosphere; | 67% |
undecanedioic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; Cooling with ice; | 76% |
Conditions | Yield |
---|---|
Stage #1: C21H25N7O With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 0.166667h; Cooling; Stage #2: undecanedioic acid In N,N-dimethyl-formamide for 0.166667h; Further stages; | 74% |
Conditions | Yield |
---|---|
With Aliquat 336; potassium carbonate In dichloromethane; water Ambient temperature; | 72% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 24h; Heating; | 70% |
Conditions | Yield |
---|---|
With dmap; 4-(dimethylamino)pyridine hydrochloride; dicyclohexyl-carbodiimide In chloroform for 14h; Heating; | 67% |
undecanedioic acid
(rac)-4-(4-fluoro-2-methoxyphenyl)-N-{3-[(S-methylsulfonimidoyl)methyl]phenyl}-1,3,5-triazin-2-amine
Conditions | Yield |
---|---|
With 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride In N,N-dimethyl-formamide at 40℃; for 3h; | 55% |
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dimethyl sulfoxide at 20℃; for 2h; | 52% |
undecanedioic acid
Conditions | Yield |
---|---|
Stage #1: (6-(6-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)-1H-benzo[d]imidazol-2-yl)methylamine tetrahydrochloride; undecanedioic acid With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0℃; for 0.166667h; Stage #2: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate In N,N-dimethyl-formamide at 0 - 20℃; Stage #3: With hydrogenchloride In methanol; water-d2 | 49.9% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 45% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 45% |
undecanedioic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dimethyl sulfoxide at 0 - 20℃; for 4h; | 43% |
undecanedioic acid
indaconitine
8-O-(14-benzoylaconine) undecanedioate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 80℃; for 7h; | 34% |
undecanedioic acid
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In tetrahydrofuran; dichloromethane at 0℃; for 2h; | 31% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 24℃; for 40h; Inert atmosphere; | 29% |
undecanedioic acid
(3E,5E,7E)-Deca-3,5,7-triene-1,10-diol
(4E,6E,8E)-1,12-Dioxa-cyclotricosa-4,6,8-triene-13,23-dione
Conditions | Yield |
---|---|
Heating; | 20% |
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine In dimethyl sulfoxide Ambient temperature; | 18% |
Conditions | Yield |
---|---|
With dmap; diisopropyl-carbodiimide In tetrahydrofuran at 20℃; for 91h; | 12% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 48h; Heating; | 8% |
undecanedioic acid
(2S,4R)-1-[(2S)-2-amino-3,3-dimethylbutanoyl]-4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide hydrochloride
Conditions | Yield |
---|---|
Stage #1: undecanedioic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 25℃; for 0.5h; Inert atmosphere; Stage #2: (2S,4R)-1-[(2S)-2-amino-3,3-dimethylbutanoyl]-4-hydroxy-N-{[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl}pyrrolidine-2-carboxamide hydrochloride In N,N-dimethyl-formamide at 25℃; for 1.5h; Inert atmosphere; | 3.4% |
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