Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Cas:5813-64-9
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Min.Order:4 Kilogram
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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,
Neopentylamine Basic information Product Name: Neopentylamine Synonyms: PIVALYLAMINE;NEOPENTYLAMINE;RARECHEM AL BW 0181;1-Propanamine, 2,2-dimethyl-;2,2-Dimethyl-1-propanamine;2,2-Dimethyl-1-propylamine;neo-C5H11NH2;2,2-DIMETHYLPROPYLAMINE CAS: 5813
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Cas:5813-64-9
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:5813-64-9
Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:5813-64-9
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Type:Lab/Research institutions
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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Min.Order:1 bottle
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Type:Lab/Research institutions
inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Cas:5813-64-9
Min.Order:0
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Type:Lab/Research institutions
inquirySupply top quality products with a reasonable price Application:api
Neopentylamine cas 5813-64-9Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Cas:5813-64-9
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inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
Trimethylacetic acid
A
2,2-dimethylpropylamine
B
2,2-dimethylpropionamide
Conditions | Yield |
---|---|
Stage #1: Trimethylacetic acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry; Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6.5h; Cooling with ice; Green chemistry; | A 74% B 26% |
Conditions | Yield |
---|---|
With ethanol; sodium | |
With ethanol; sodium; toluene | |
With lithium aluminium tetrahydride; diethyl ether |
Conditions | Yield |
---|---|
With nickel; ethylene glycol at 105℃; Hydrogenation; | |
With hydrogen In tetrahydrofuran at 140℃; under 30003 Torr; for 2.25h; |
N,N'-bis(2,2-dimethylpropylidene)-2,2-dimethyl-1,1-propanediamine
A
2,2-dimethylpropylamine
B
di(neo-pentyl)amine
Conditions | Yield |
---|---|
With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |
2,2-dimethylpropionamide
A
2,2-dimethylpropylamine
B
2,2-dimethyl-propanol-1
Conditions | Yield |
---|---|
With ethanol; sodium | |
With sec.octyl alcohol; sodium | |
With dodecacarbonyl-triangulo-triruthenium; hydrogen; molybdenum hexacarbonyl In 1,2-dimethoxyethane at 160℃; under 75007.5 Torr; for 16h; Inert atmosphere; |
tert-butylisonitrile
A
N-methyl-tert-butylamine
B
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With nickel at 170 - 180℃; Hydrogenation; |
Conditions | Yield |
---|---|
With ammonium amalgam | |
Multi-step reaction with 2 steps 1: NH3 2: nickel kieselguhr; methylcyclohexane / 100 - 125 °C / 73550.8 - 110326 Torr / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: ZnCl2 2: LiAlH4 / diethyl ether View Scheme |
1-neopentylurea
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
(hydrolysis); |
α-Trimethyl-siloxy-neopentylazid
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether |
Conditions | Yield |
---|---|
With ammonia; hydrogen; iron at 230 - 250℃; under 22501.8 - 37503 Torr; | 35 % Chromat. |
Multi-step reaction with 2 steps 1: Na2Cr2O7; H2SO4 2: ammonium amalgam View Scheme | |
With dodecacarbonyl-triangulo-triruthenium; 4,5-bis((diisopropylphosphanyl)methyl)acridine; ammonia In tert-Amyl alcohol at 150℃; for 21h; Temperature; Inert atmosphere; Schlenk technique; Autoclave; |
pivalaldehyde
A
2,2-dimethylpropylamine
B
2,2-dimethyl-propanol-1
C
Trimethylacetic acid
tert-butyl isocyanide
ethanol
toluene
A
Isobutane
B
2,2-dimethylpropylamine
C
sodium cyanide
2,2-dimethylpropionaldehyde oxime
ethylene glycol
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
at 105℃; Hydrogenation; |
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With sodium hypobromide; water |
tert-butylisonitrile
A
N-methyl-tert-butylamine
B
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
at 170 - 180℃; Hydrogenation; |
diethyl ether
N,N'-bis(2,2-dimethylpropylidene)-2,2-dimethyl-1,1-propanediamine
A
2,2-dimethylpropylamine
B
di(neo-pentyl)amine
Conditions | Yield |
---|---|
at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |
N,N'-bis(2,2-dimethylpropylidene)-2,2-dimethyl-1,1-propanediamine
ethanol
A
2,2-dimethylpropylamine
B
di(neo-pentyl)amine
Conditions | Yield |
---|---|
at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |
N,N'-bis(2,2-dimethylpropylidene)-2,2-dimethyl-1,1-propanediamine
methyl cyclohexane
A
2,2-dimethylpropylamine
B
di(neo-pentyl)amine
Conditions | Yield |
---|---|
at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |
2,2-dimethylpropionamide
A
tert-butyl isocyanide
B
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With sodium tetrahydroborate In diethylene glycol dimethyl ether at 162℃; for 2h; Title compound not separated from byproducts.; | A 55 % Chromat. B 44 % Chromat. |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: water; ammonia 2: sodium; sec.octyl alcohol View Scheme |
tert-butyl isocyanide
(C5(CH3)5)2ScNHCH2C(CH3)3
A
(C5(CH3)5)2ScNC(NHCH2C(CH3)3)C(CH3)3
B
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With hydrogen In benzene-d6 High Pressure; NMR tube charged with (C5Me5)2ScNHCH2CMe3 and C6D6, cooled to 77 K, t-BuCN condensed in, 700 torr of H2 introduced, sealed, reacted at 25°C and 4 atm of H2 for 17 h, heated to 80°C for further 24 h; not isolated; detected by NMR; |
tert-butyl isocyanide
B
2,2-dimethylpropylamine
C
2,2-dimethylpropan-1-imine
Conditions | Yield |
---|---|
With Os(hydride)6(triisopropylphosphine)2; hydrogen In (2)H8-toluene at 100℃; under 3000.3 Torr; for 24h; | A 65 %Spectr. B 15 %Spectr. C 20 %Spectr. |
2,2-dimethylpropylamine
pyridin-4-yl isothiocyanate
N-neo-pentyl-N'-4-pyridylthiourea
Conditions | Yield |
---|---|
In diethyl ether at 0℃; | 100% |
2,2-dimethylpropylamine
N-tert-butyloxycarbonylpiperidin-4-one
tert-butyl 4-[(2,2-dimethylpropyl)amino]piperidine-1-carboxylate
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In ethanol under 3102.97 Torr; for 3h; | 100% |
Stage #1: 2.2-dimethylpropylamine; N-tert-butyloxycarbonylpiperidin-4-one With triethylamine; zinc(II) chloride In methanol at 65℃; for 6h; Stage #2: With sodium cyanoborohydride In methanol at 0 - 25℃; for 17h; | 88% |
With sodium tetrahydroborate In methanol at 0 - 20℃; for 42h; |
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
In benzene-d6 byproducts: pyridine; air and H2O free atmosphere, NMR tube; 45°C (1 h); evapn. (vac.); detd. by (1)H NMR spectroscopy; | 100% |
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
In benzene-d6 air and H2O free atmosphere, NMR tube; room temp. (24 h); evapn. (vac.); detd. by (1)H NMR spectroscopy; | 100% |
Conditions | Yield |
---|---|
Stage #1: 4-bromo-isophthalic acid With triethylamine In dichloromethane for 0.5h; Stage #2: With 1,1'-carbonyldiimidazole In dichloromethane for 1.08333h; Stage #3: 2.2-dimethylpropylamine In dichloromethane for 2.5h; | 100% |
2,2-dimethylpropylamine
3-bromonaphthalic-1,8-anhydride
5-bromo-2-neopentyl-1H-benzo[de]isoquinoline-1,3(2H)-dione
Conditions | Yield |
---|---|
In 1,4-dioxane at 100℃; for 4h; | 100% |
2,2-dimethylpropylamine
ethyl 5-(2-(tert-butyl)-6-(((trifluoromethyl)sulfonyl)oxy)pyridin-4-yl)-1-(cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylate
ethyl 5-(2-(tert-butyl)-6-(neopentylamino)pyridin-4-yl)-1-(cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylate
Conditions | Yield |
---|---|
With palladium diacetate; sodium t-butanolate; DavePhos In toluene at 110℃; for 2h; Inert atmosphere; | 100% |
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
In toluene at 20℃; for 0.166667h; Glovebox; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In chloroform at 50℃; for 1h; Inert atmosphere; | 100% |
sarcosine-N-carboxyanhydride
2,2-dimethylpropylamine
tyrosine
D-phenylalanine N-carboxyanhydride
Conditions | Yield |
---|---|
Stage #1: sarcosine-N-carboxyanhydride; 2.2-dimethylpropylamine In N,N-dimethyl-formamide for 20h; Darkness; Stage #2: tyrosine; D-phenylalanine N-carboxyanhydride In N,N-dimethyl-formamide at 25℃; for 24h; | 99.3% |
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In DMF (N,N-dimethyl-formamide) at 20℃; for 18h; | 99% |
3-(6-chloro-pyrimidin-4-ylamino)-4,N-dimethyl-benzamide
2,2-dimethylpropylamine
3-[6-(2,2-Dimethyl-propylamino)-pyrimidin-4-ylamino]-4,N-dimethyl-benzamide
Conditions | Yield |
---|---|
In dimethyl sulfoxide | 99% |
Conditions | Yield |
---|---|
With triethylamine In butan-1-ol at 110℃; for 12h; Inert atmosphere; | 99% |
With N-ethyl-N,N-diisopropylamine In butan-1-ol at 95℃; |
2,2-dimethylpropylamine
2-tert-butoxycarbonylamino-succinic acid 1-benzyl ester
Conditions | Yield |
---|---|
Stage #1: 2-tert-butoxycarbonylamino-succinic acid 1-benzyl ester With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 0.5h; Stage #2: 2.2-dimethylpropylamine With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 3h; | 99% |
With 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In dichloromethane at 25℃; for 24h; |
2,2-dimethylpropylamine
2,4-dichloropyrimidine-6-carboxylic acid chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -78 - 0℃; | 99% |
2,4-dichloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In ethanol at 80℃; for 12h; | 98.4% |
2-Chloro-3-nitropyridine
2,2-dimethylpropylamine
N-neopentyl-3-nitropyridin-2-amine
Conditions | Yield |
---|---|
With sodium carbonate In ethanol at 20℃; Inert atmosphere; | 98.1% |
With sodium carbonate In N,N-dimethyl-formamide at 90℃; |
2,2-dimethylpropylamine
propyl N-cyano-3-pyridinecarboximidate
Conditions | Yield |
---|---|
In methanol Ambient temperature; | 98% |
2,2-dimethylpropylamine
methyl (2S,5S)-{5-methoxycarbonylmethyl-3,6-dioxo-1,4-bis[(phenylmethylcarbamoyl)methyl]piperazin-2-yl}acetate
Conditions | Yield |
---|---|
Stage #1: methyl (2S,5S)-{5-methoxycarbonylmethyl-3,6-dioxo-1,4-bis[(phenylmethylcarbamoyl)methyl]piperazin-2-yl}acetate With sodium hydroxide In methanol Hydrolysis; Stage #2: With 2,6-dimethylpyridine; isobutyl chloroformate In N,N-dimethyl-formamide at -15℃; Acylation; Stage #3: 2.2-dimethylpropylamine In N,N-dimethyl-formamide at -15 - 20℃; Acylation; | 98% |
Stage #1: methyl (2S,5S)-{5-methoxycarbonylmethyl-3,6-dioxo-1,4-bis[(phenylmethylcarbamoyl)methyl]piperazin-2-yl}acetate With sodium hydroxide In methanol Hydrolysis; Stage #2: With 2,6-dimethylpyridine; isobutyl chloroformate In N,N-dimethyl-formamide at -15℃; Acylation; Stage #3: 2.2-dimethylpropylamine In N,N-dimethyl-formamide at -15 - 20℃; Acylation; Further stages.; | 98% |
methyl 2-bromo-1-methyl-1H-1,3-benzodiazole-5-carboxylate
2,2-dimethylpropylamine
methyl 2-[(2,2-dimethylpropyl)amino]-1-methyl-1H-benzimidazole-5-carboxylate
Conditions | Yield |
---|---|
With cesium fluoride In dimethyl sulfoxide at 115℃; for 7h; Microwave irradiation; | 98% |
ethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylate
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 90℃; for 24h; | 98% |
ethyl 7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylate
2,2-dimethylpropylamine
Conditions | Yield |
---|---|
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 90℃; for 24h; | 98% |
2,2-dimethylpropylamine
4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran
acetyl chloride
A
N-neopentyl-acetamide
B
(2,2-Dimethyl-propyl)-ethyl-amine
Conditions | Yield |
---|---|
With triethylamine | A n/a B 98% |
With triethylamine | A n/a B 98% |
pyridine-2-carbaldehyde
2,2-dimethylpropylamine
NC5H4-2-C(H)=N(neo-Pent)
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane for 2h; Glovebox; | 98% |
Conditions | Yield |
---|---|
at 20℃; for 17h; Inert atmosphere; Schlenk technique; Glovebox; | 98% |
sarcosine-N-carboxyanhydride
2,2-dimethylpropylamine
tyrosine
D-phenylalanine N-carboxyanhydride
Conditions | Yield |
---|---|
Stage #1: sarcosine-N-carboxyanhydride; 2.2-dimethylpropylamine In N,N-dimethyl-formamide for 20h; Darkness; Stage #2: tyrosine; D-phenylalanine N-carboxyanhydride In N,N-dimethyl-formamide at 25℃; for 24h; | 97.7% |
2,2-dimethylpropylamine
N-tert-butoxycarbonyl aspartic acid tert-butyl ester
Boc-neopentyl-Asn-O-tBu
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; | 97% |
Stage #1: N-tert-butoxycarbonyl aspartic acid tert-butyl ester With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In N,N-dimethyl-formamide for 0.25h; Stage #2: 2.2-dimethylpropylamine In N,N-dimethyl-formamide for 4h; | 90% |
With 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In DMF (N,N-dimethyl-formamide) at 20℃; for 4h; | 81% |
Conditions | Yield |
---|---|
In methanol at -30 - 20℃; for 16h; | 97% |
2,2-dimethylpropylamine
2-(tert-butyl)-6-(diethoxymethyl)-3-fluoro-N-tritylpyridin-4-amine
Conditions | Yield |
---|---|
Stage #1: 2.2-dimethylpropylamine; N-(5,5-diethoxy-1,1,1-trifluoropent-3-yn-2-ylidene)-1,1,1-triphenylmethanamine In dimethyl sulfoxide at 20 - 30℃; for 0.5h; Stage #2: With caesium carbonate In dimethyl sulfoxide at 100℃; for 16h; | 97% |
2,2-dimethylpropylamine
HU-331
Conditions | Yield |
---|---|
With air In ethanol at 20℃; for 20h; | 97% |
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