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 according to the contract research and development services for t
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryProduct informations Product Name 2-Picoline CAS No. 109-06-8 Appearance
Hebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
1.strict Quality control: Strictly in accordance with Chinese GMP(2010 version), guidelines issued by FDA,EDQM, and ICH relevant regulations, we have established a sound quality assurance system, implementing regular supervision and management in
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2-Picoline Basic information Product Name: 2-Picoline Synonyms: ALPHA-PICOLINE;ALPHAP;2-METHYLPYRIDINE;2-PICOLINE;.alpha.-Methylpyridine;2-methyl-pyridin;ai3-2409;alpha-Methylpyridine
Cas:109-06-8
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inquiryProduct:2-Picoline CASNO.:109-06-8 Molecular formula:C6H7N Molecular weight:93.13 EINECS: 203-643-7 Diagnosis-related group: Pesticide intermediates. Plant growth regulator intermediates Appearance:Colorless Liquid Storage: Store in cool an
Advantages: Hubei XinRunde Chemical Co., Ltd is a renowned pharmaceutical manufacturer. We can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. Never stop striving to offer our best s
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inquiryAbout us Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad.
Appearance:white powder Storage:Store in a cool,dry place and keep away from direct strong light Package:packaged in foil bags or tins Application:Use only for laboratory research Transportation:Sea,Air,DHL/TNT/FEdex/UPS/EMS Por
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
J&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
Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Zibo Hangyu Biotechnology Development 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 chemi
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inquiryHunan 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
ProName: 2-Picoline suppliers in China CasNo: 109-06-8 Molecular Formula: C6H7N Appearance: colourless to yellow liquid with an un... Application: Used as medicine, pesticide intermedia... DeliveryTime: prompt PackAge
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
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inquiryHangzhou 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
Name: 2-Picoline. Synonyms:2-Methylpyidine;2-PICOLINE98%;2-methylpyridine(2-Picoline);2-Picoline,98+%;Pyridine,Reagent;2-methylpyridine,2-pieoline;2-Picoline(2-Methylpyridine);NSC-3409 CAS No: 109-06-8. Molecular formula: C6H7N. Molecular w
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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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inquiryCapability on chemical synthesis1. Beijing High-Tech Enterprises2. Strong R&D Team3. 8 years of experiences in R & D of high-tech Catalyst;4. 5000 production techniques, 69 items of national patents, and 360 kinds of products on sales;5. The producti
Superior quality, moderate price & quick delivery. Appearance:colourless to yellow liquid with an unpleasant smell Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:as per your request Application:Used as Pharma
Product Name3-Amino-4-(trifluoromethyl)pyridine CAS 175204-80-5 MF C6H5F3N2 MW 162.11 Product Name3-Amino-4-(trifluoromethyl)py…
Hangzhou Dingyan Chem is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals. We could give you: 1.Best qualit
ISO/factory/goodqualityAppearance:off white Storage:Dry,cool place Package:drum Application:active pharmaceutical ingredients Transportation:by air/sea/express Port:shenzhen/shanghai
high 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
propene
A
α-picoline
Conditions | Yield |
---|---|
<10 min, 23°C, 1 atm.; monitored by NMR; | A n/a B 100% |
Conditions | Yield |
---|---|
With benzyl alcohol at 120℃; for 6h; Inert atmosphere; | 99% |
With cis-Cyclooctene; trans-dioxo(5,10,15,20-tetramesitylporphirinato)ruthenium(VI) In benzene at 80℃; for 15h; | 96% |
With diphosphorus tetraiodide In dichloromethane Heating; 10-20 min; | 95% |
Conditions | Yield |
---|---|
at 150℃; for 22h; Autoclave; | 94.3% |
With decaethylene glycol mono n-hexadecyl ether; cyclopentadienyl-cyclooctadienyl-cobalt(I) In water for 4h; Ambient temperature; Irradiation; | 18% |
(η5-cyclopentadienyl)-η4-cycloocta-1,5-dienecobalt(I) at 40℃; for 2h; Irradiation; Yield given; | |
trimethylsilyl modified Cp-CO catalyst at 130 - 152℃; under 15001.2 Torr; for 2h; | |
η5-cyclopentadienylbis(ethene)cobalt at 40℃; for 3h; Product distribution; in the dark; variation of reaction time, temperature, catalyst. The influence of light and irradiation was investigated.; |
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; cesium fluoride In 2-pentanol at 100℃; for 18h; Inert atmosphere; | A 93.1% B 6.9% |
pyridine
A
piperidine
B
α-picoline
C
1,5-di-(1-piperidyl)pentane
Conditions | Yield |
---|---|
With hydrogen; Ni-Cr catalyst at 160℃; under 30400 Torr; for 8h; Product distribution; temperatures from 140 to 192 deg C, pressure 20 to 65 atm, reaction time 5 - 8 h; | A 91.8% B n/a C 0.1% |
Conditions | Yield |
---|---|
With Fe-MnOx-Yb at 475℃; Gas phase; | 89.5% |
nickel(II) nitrate for 8h; Ambient temperature; Irradiation; | 37.1% |
With nano-diatomite modified magnesium aluminum hydrotalcite at 140 - 500℃; Temperature; |
Conditions | Yield |
---|---|
With samarium diiodide; phosphoric acid In tetrahydrofuran for 0.000555556h; Ambient temperature; | 88% |
benzyltri(2-(6-methylpyridyl))phosphonium bromide
A
α-picoline
B
6,6'-dimethyl-2,2'-bipyridine
Conditions | Yield |
---|---|
With hydrogenchloride In water for 10h; Heating; | A 68% B 87% C n/a |
With hydrogenchloride In water for 10h; Product distribution; Heating; variation of pH, temp. and time; | A 68% B 87% C n/a |
With hydrogenchloride In water for 10h; Heating; | A 68% B 68% C n/a |
N-cetyl-α-methylpyridinium iodide
α-picoline
Conditions | Yield |
---|---|
With triethylammonium hydrogensulfite at 150℃; for 30h; Mechanism; | 86% |
triphenyl-(2-pyridylmethyl)phosphonium chloride
α-picoline
Conditions | Yield |
---|---|
With potassium tert-butylate; benzyl alcohol In tetrahydrofuran at 40℃; for 6h; Inert atmosphere; | 80% |
2-pyridineacetic acid
α-picoline
Conditions | Yield |
---|---|
With potassium carbonate In chloroform at 20℃; for 24h; Irradiation; Inert atmosphere; | 79% |
Conditions | Yield |
---|---|
With Raney nickel at 180℃; under 51716.2 Torr; for 0.5h; Concentration; Flow reactor; Green chemistry; regioselective reaction; | 78% |
Conditions | Yield |
---|---|
With Ra-Ni for 212h; Reflux; regioselective reaction; | 71% |
α-picoline
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); sodium isopropylate; 1,3-bis[(2,6-diisopropyl)phenyl]imidazolinium chloride In 2-methyltetrahydrofuran at 80℃; for 12h; Green chemistry; | 71% |
With bis(tricyclohexylphosphine)nickel(II) dichloride; potassium iodide; zinc In 1,4-dioxane; methanol at 60℃; for 20h; Inert atmosphere; chemoselective reaction; |
Conditions | Yield |
---|---|
Stage #1: 2-iodopyridine; bis(iodozinc)methane With triphenylphosphine; nickel dichloride In tetrahydrofuran at 40℃; Stage #2: With hydrogenchloride In tetrahydrofuran; water Reagent/catalyst; chemoselective reaction; | 71% |
Conditions | Yield |
---|---|
With hydrogen In para-xylene at 120℃; under 750.075 Torr; for 24h; Glovebox; Sealed tube; chemoselective reaction; | 71% |
Conditions | Yield |
---|---|
In perchloric acid addn. of Na2CO3;; | A 70% B 30% |
In perchloric acid |
Conditions | Yield |
---|---|
With hydrogen; GIPKh-105 copper-chromium catalyst at 200℃; Product distribution; Mechanism; other isomeric pyridinecarboxaldehydes; var. temp.; | A 14% B 66% |
2-chloromethylpyridine
benzaldehyde
A
α-picoline
B
1-phenyl-2-pyridin-2-yl-ethanol
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; silver nitrate; zinc In water at 30℃; for 1h; | A 51% B 66% |
Conditions | Yield |
---|---|
With [IrCl(CO)(PPh3)2]; hydrazine hydrate; potassium hydroxide In methanol at 160℃; for 3h; Wolff-Kishner Reduction; Sealed tube; | 62% |
With [IrCl(CO)(PPh3)2]; hydrazine hydrate; potassium hydroxide In methanol at 160℃; for 3h; Sealed tube; | 62% |
With hydrazine hydrate; C23H40MnNO2P2; potassium tert-butylate In tert-butyl alcohol at 115℃; for 48h; Wolff-Kishner Reduction; Green chemistry; | 26% |
Conditions | Yield |
---|---|
With ammonia; Pb(5.3percent)/borotitano silicate at 420℃; for 1h; Product distribution / selectivity; Molecular sieve; | A 2.4% B 61.3% C 21.6% |
With ammonia; Pb/SnS-1B at 395℃; Product distribution / selectivity; | A 1% B 53.4% C 22.3% |
With ammonia; titanium-silicate catalyst (sample C) at 250 - 400℃; Conversion of starting material; | A 0.88% B 53.44% C 20.55% |
formaldehyd
acetaldehyde
A
pyridine
B
α-picoline
C
picoline
D
3-Methylpyridine
Conditions | Yield |
---|---|
With Pb-ZSM-5 zeolite; ammonia In gas | A 60% B 7% C 4% D 8% |
With Co-ZSM-5 zeolite; ammonia In gas | A 57% B 6% C 8% D 7% |
With Ag-ZSM-5 zeolite; ammonia In gas | A 42% B 3% C 6% D 11% |
With pentasil zeolite H-ZSM-5; ammonia In gas at 450℃; Product distribution; synthesis of pyridine bases over ion-exchanged pentasil zeolite; var. zeolites, var. Si/Al atomic ratio; | A 42% B 3% C 5% D 11% |
pyridine-2-carboxylic acid amide
A
α-picoline
B
2-Methylpiperidin
Conditions | Yield |
---|---|
With hydrogenchloride; samarium for 0.166667h; Ambient temperature; | A 13% B 60% |
Conditions | Yield |
---|---|
With n-butyllithium; 2-(N,N-dimethylamino)ethanol 1.) hexane, -78 deg C, 1 h, 2.) THF, -78 deg C, 1 h; | A 60% B 16 % Chromat. |
acetone
acetylene
A
α-picoline
B
2,6-dimethylpyridine
C
2,4,6-trimethyl-pyridine
D
2,4-lutidine
Conditions | Yield |
---|---|
With ammonia; MG-4 at 375℃; under 760 Torr; | A 6.3% B 7.3% C 58.3% D 5.9% |
With ammonia; MG-4 at 375℃; under 760 Torr; Product distribution; other catalysts; | A 6.3% B 7.3% C 58.3% D 5.9% |
With ammonia; MG-4 at 350℃; under 760 Torr; | A 6.2% B 15.6% C 36.4% D 6.8% |
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at 40℃; for 6h; | A 58% B 26% |
4-chIoro-2-methylpyridine
bis(pinacol)diborane
A
α-picoline
B
2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Conditions | Yield |
---|---|
With bis(1,3-dimesityl-1H-imidazol-2(3H)-ylidene)nickel(0); potassium methanolate In hexane at 25℃; for 6h; Inert atmosphere; Irradiation; | A 10 %Chromat. B 55% |
2-methylpyridine N-oxide
N,N-Dimethylthiocarbamoyl chloride
A
α-picoline
Conditions | Yield |
---|---|
In acetonitrile at 81℃; for 4h; | A 52% B 3% C 5% |
Conditions | Yield |
---|---|
With water-d2 In water-d2 | A 50% B 50% |
With D2O In water-d2 |
Conditions | Yield |
---|---|
In toluene at 110℃; for 19h; | 100% |
In acetone for 8h; Heating; | 51% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; Na12[WZn3(H2O)2(ZnW9O34)2] at 75℃; for 7h; | 100% |
With 2,2,2-Trifluoroacetophenone; dihydrogen peroxide; acetonitrile In tert-butyl alcohol at 20℃; for 18h; Green chemistry; chemoselective reaction; | 99% |
With dihydrogen peroxide In acetic acid at 70 - 75℃; for 24h; Oxidation; | 98% |
Conditions | Yield |
---|---|
100% | |
In acetone Reflux; | 100% |
In toluene for 14h; Inert atmosphere; Reflux; | 72% |
Conditions | Yield |
---|---|
With phenyllithium In diethyl ether for 2.5h; Heating; | 100% |
α-picoline
2,4-dimethylpentan-3-one
2,4-dimethyl-3-(pyridin-2-ylmethyl)pentan-3-ol
Conditions | Yield |
---|---|
Stage #1: α-picoline With tert.-butyl lithium In tetrahydrofuran; pentane at -30℃; Stage #2: 2,4-dimethylpentan-3-one In tetrahydrofuran; pentane at -30 - 20℃; Stage #3: With water In tetrahydrofuran; pentane | 100% |
Stage #1: α-picoline With n-butyllithium In tetrahydrofuran; hexane at -78 - -50℃; for 1h; Inert atmosphere; Stage #2: 2,4-dimethylpentan-3-one In tetrahydrofuran; hexane at -50℃; for 2h; Inert atmosphere; | 91% |
Stage #1: α-picoline With n-butyllithium In tetrahydrofuran; hexane at -78 - -50℃; for 1h; Inert atmosphere; Stage #2: 2,4-dimethylpentan-3-one In tetrahydrofuran; hexane at -50℃; for 2h; Inert atmosphere; Stage #3: With water In tetrahydrofuran; hexane Inert atmosphere; | 90% |
α-picoline
di-μ-chloro-dichloro-bis[η5-(perfluorobutyl)tetramethylcyclopentadienyl]-dirhodium(III)
dichloro-(perfluorohexyl)tetramethylcyclopentadienyl-(2-methylpyridine)-rhodium(III)
Conditions | Yield |
---|---|
In chloroform (Ar); methylpyridine was added to soln. of Rh complex in CHCl3; mixt. was stirred for 2 h at room temp.; evapd.; dried (vac.); | 100% |
α-picoline
dicyclohexyl ketone
1,1-dicyclohexyl-2-(pyridin-2-yl)ethanol
Conditions | Yield |
---|---|
Stage #1: α-picoline With n-butyllithium In tetrahydrofuran; hexane at -78 - -20℃; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexane at -20℃; Inert atmosphere; Stage #3: With water; ammonium chloride In tetrahydrofuran; hexane | 100% |
α-picoline
(bromomethyl)pentafluorobenzene
N-(pentafluorobenzyl)-2-methylpyridinium bromide
Conditions | Yield |
---|---|
In chloroform at 20℃; for 24h; | 100% |
α-picoline
4-heptadecafluorooctylaniline
Conditions | Yield |
---|---|
With sodiumsulfide nonahydrate; sulfur for 72h; Reflux; | 100% |
Conditions | Yield |
---|---|
In 1,4-dioxane at 101℃; for 16h; Inert atmosphere; | 100% |
α-picoline
Conditions | Yield |
---|---|
Stage #1: α-picoline With potassium tert-butylate at -35℃; for 0.333333h; Stage #2: With n-butyllithium In hexane at -35 - 20℃; for 4h; | 100% |
With n-butyllithium; potassium tert-butylate In hexane at 20℃; for 1h; Schlenk technique; Glovebox; | 63% |
α-picoline
Conditions | Yield |
---|---|
for 0.0833333h; Reflux; | 100% |
Conditions | Yield |
---|---|
at 20℃; for 0.166667h; Glovebox; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; | 100% |
α-picoline
2-Bromo-4'-methoxyacetophenone
2-(4-methoxyphenyl)-indolizine
Conditions | Yield |
---|---|
Stage #1: α-picoline; 2-Bromo-4'-methoxyacetophenone In acetone for 1h; Heating; Stage #2: With potassium carbonate for 5h; | 99% |
α-picoline
tetrachloro-cyclopent-4-ene-1,3-dione
Conditions | Yield |
---|---|
In formic acid at 100℃; Product distribution; CH3CO2H,CF3CO2H; | 99% |
With acetic acid Ambient temperature; | 87.4% |
α-picoline
ethyl bromoacetate
1-(2-ethoxy-2-oxoethyl)-2-methylpyridin-1-ium bromide
Conditions | Yield |
---|---|
In ethanol at 60 - 80℃; for 20h; | 99% |
In tetrahydrofuran at 80℃; for 12h; Inert atmosphere; | 92% |
for 16h; Reflux; | 90% |
α-picoline
(1R,2S,5R)-1-(chloromethoxy)-2-isopropyl-5-methylcyclohexane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin quaternization; | 99% |
Conditions | Yield |
---|---|
Stage #1: α-picoline With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -5℃; for 0.5h; Stage #2: phenanthrene-3-carbaldehyde In tetrahydrofuran; hexane at 20℃; for 0.5h; Further stages.; | 99% |
α-picoline
thallium(I) pentafluorobenzoate
(SP-4-3)-dichlorido(N,N-dimethyl-ethane-1,2-diamine)platinum(II)
Pentafluorobenzene
b-chloro-c(N),d(N')-{N,N-dimethyl-N'-(2,3,5,6-tetrafluorophenyl)ethane-1,2-diaminato(1-)}-a-(2-methylpyridine)platinum(II)
B
carbon dioxide
Conditions | Yield |
---|---|
In further solvent(s) Heating under stirring (110-115°C, N2, 120 min, 2-methylpyridine).; Cooling, evapn. to dryness (vacuum), washed (ether, petrol), dried, extraction with acetone, filtn. of TlCl, evapn. to dryness, washed (cold ethanol), elem. anal.; | A 28% B 99% |
α-picoline
Conditions | Yield |
---|---|
In neat (no solvent) standing in vapor of amine (room temp., 2 days); | 99% |
In benzene addn. of amine to Fe-complex; distn. off of excess amine and solvent (after 24 h), drying (vac., room temp.); |
α-picoline
trans-[Pd(AsPh3)2(3,5-dichlorotrifluorophenyl)2]
cis-[Pd(2-picoline)2(3,5-dichlorotrifluorophenyl)2]
Conditions | Yield |
---|---|
In dichloromethane excess of picoline, stirring for 30 min; evapn., washing (hexane), drying; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In dichloromethane excess of picoline, stirring for 30 min; evapn., washing (hexane), drying; elem. anal.; | 99% |
α-picoline
trans-chloromethylbis(dimethylsulfoxide)platinum(II)
cis(C,N)-chloromethyl(dimethyl sulfoxide)(2-methylpyridine)platinum(II)
Conditions | Yield |
---|---|
In dichloromethane stirring stoich. amts. for 30 min; addn. of pentane, pptn. on cooling, collection (filtration), washing (cold pentane), drying (vac.); elem. anal.; | 99% |
α-picoline
4-Cyanochlorobenzene
bis(trichloromethyl) carbonate
3-(4-chlorophenyl)pyrido[1,2-c]pyrimidin-1-one
Conditions | Yield |
---|---|
Stage #1: α-picoline With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -70℃; for 1h; Inert atmosphere; Stage #2: 4-Cyanochlorobenzene In tetrahydrofuran; hexane at -70 - 20℃; Inert atmosphere; Stage #3: bis(trichloromethyl) carbonate With triethylamine In tetrahydrofuran; hexane at 20℃; for 2h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
at 20℃; for 504h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With C50H63NO2Zr; trityl tetrakis(pentafluorophenyl)borate In chlorobenzene at 100℃; for 6h; Inert atmosphere; Glovebox; | 99% |
With tris(pentafluorophenyl)borate; C42H51N3PSc In chlorobenzene at 100℃; for 15h; Inert atmosphere; Schlenk technique; Glovebox; | 82% |
With C23H29N2Sc; triphenylcarbenium tetra(pentafluorophenyl)borate at 70℃; Schlenk technique; Inert atmosphere; |
Conditions | Yield |
---|---|
With C50H63NO2Zr; trityl tetrakis(pentafluorophenyl)borate In chlorobenzene at 100℃; for 6h; Inert atmosphere; Glovebox; | 99% |
With tris(pentafluorophenyl)borate; C42H51N3PSc In chlorobenzene at 100℃; for 15h; Inert atmosphere; Schlenk technique; Glovebox; | 81% |
With C23H29N2Sc; triphenylcarbenium tetra(pentafluorophenyl)borate at 70℃; Schlenk technique; Inert atmosphere; |
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