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Cas:71-36-3
Min.Order:1 Kilogram
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Type:Manufacturers
inquiryDayangchem'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:71-36-3
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryT he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:White or
Cas:71-36-3
Min.Order:1 Kilogram
Negotiable
Type:Manufacturers
inquiry1-Butanol Product Name: 1-Butanol Synonyms: butan-1-ol; Butyric alcohol; Butyl alcohol; n-Butanol; n-butyl alcohol; Propylcarbinol; Normal Butanol; Natural Butyl Alcohol; Butanol CAS RN.:
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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 carb
Cas:71-36-3
Min.Order:1 Metric Ton
FOB Price: $1.0 / 3.0
Type:Trading Company
inquiry1-Butanol Basic information Characteristics and history of discovery Preparation of water saturated 1-butanol solution Content AnalysisReference quality standards Toxicity Limited use The maximum allowable amount of food a
Cas:71-36-3
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryProduct Description Product website: http://www.finerchem.com Product Name 1-Butanol CAS No. 71-36-3 Appear
Chemical Names: 1-butanol; N-butanol; Butyl alcohol; Butanol; Butan-1-ol; N-butyl alcohol; Product name: N-Butanol CAS Number 71-36-3 Molecular formula C4H100 Appearance: Colorless liquid Storage:Preserve in well-closed, light-resistant and a
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. At presen
Cas:71-36-3
Min.Order:25 Milliliter
FOB Price: $16.0 / 20.0
Type:Trading Company
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Company information: Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in carbomer,carbopol,lead acetate,meglumine diphenyl ethylamine and other chemical raw materials and chemical reagents research and development production ente
Cas:71-36-3
Min.Order:1 Kilogram
FOB Price: $10.0 / 30.0
Type:Trading Company
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:71-36-3
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryAppearance:White or off-white Solid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Organic synthesis Transportation:Common products:Sea/Air/Courier Dangerous Che
Hangzhou 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
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
Cas:71-36-3
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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,
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
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
High purity, high success rate, short cycle and moderate priceAppearance:White powder solid Storage:Negative 20 degrees Celsius Package:5mg, 10mg 100mg, 1gram Application:Applied to various scientific research
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
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
high purity, manufacturer Application:Intermediate
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:71-36-3
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep 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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
Chinese supplier suppliers manufacturer factory of n-Butanol 1-Butanol Application:Chinese supplier suppliers manufacturer factory of n-Butanol 1-Butanol
Cas:71-36-3
Min.Order:0
Negotiable
Type:Other
inquiryConditions | Yield |
---|---|
With Ipc2BOH In pentane at 25℃; for 6h; | 100% |
With Ca2>2*THF In hexane at 20℃; for 0.5h; other carbonyl compounds, var. calcium tetrakis(alkoxy)alanates, solvents, times, temp.; | 99% |
With hydrogen; aluminum oxide; copper at 150℃; | 99% |
Conditions | Yield |
---|---|
With hydrogenchloride In acetone at 20℃; for 0.25h; Product distribution; other alkyl formates; | 100% |
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h; | 75% |
With water; tetraphenylphosphonium bromide; triphenylphosphine; potassium hydroxide In dibutyl ether at 25℃; for 0.166667h; | 11% |
Conditions | Yield |
---|---|
With lithium dihydrido borata-bicyclo[3.3.0]nonane In tetrahydrofuran at 15℃; for 0.25h; Product distribution; with other oxiranes; | A 99% B 1% |
With zeolite supported zinc borohydride In tetrahydrofuran at 20℃; for 12h; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With methanol; DOWEX 50 W-X2 cation exchange resin at 40℃; for 1.13333h; | A n/a B 99% |
Conditions | Yield |
---|---|
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A 99% B n/a |
Tributoxyoxovanadium
(3bR,4aR)-2-(3,4,4-trime-3b,4,4a,5-tetrahydrocyclopropa[3,4]cyclopenta[1,2-c]pyrazol-1-yl)-ethanol
17O-water
B
butan-1-ol
Conditions | Yield |
---|---|
In dichloromethane compd. prepd. by react. VO(On-Bu)3 with ligand in CH2Cl2; H2(17)O added to soln.; detn. by NMR; | A 99% B n/a |
Conditions | Yield |
---|---|
With 0.5%Pd/TiO2; isopropyl alcohol In water at 24.84℃; for 2h; Inert atmosphere; Sealed tube; Irradiation; | A 99% B 99% |
Conditions | Yield |
---|---|
With hydrogen; Cu-based catalyst at 190℃; Product distribution; Further Variations:; Temperatures; reaction in vapour phase, fixed bed reactor; | A 98.8% B 0.8% |
maleic acid
A
tetrahydrofuran
B
4-butanolide
C
methanol
D
Butane-1,4-diol
E
malic acid
F
succinic acid
G
acetic acid
H
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; 0.5percent Pd on Rutile TiO2 at 110℃; Product distribution / selectivity; | A 0.45% B 0.06% C 0% D 0.21% E 0.36% F 98.73% G 0.04% H 0.08% |
Conditions | Yield |
---|---|
With hydrogen at 265℃; for 3480h; Reagent/catalyst; Time; | 98% |
With water In aq. phosphate buffer at 20℃; pH=7.4; Electrolysis; Inert atmosphere; Enzymatic reaction; | 98.5% |
With diphenylamine borane In tetrahydrofuran 1.) 0 deg C, 1 h, 2.) 20 deg C, 1 h; | 61% |
maleic acid
A
tetrahydrofuran
B
4-butanolide
C
Butane-1,4-diol
D
4-hydroxybutanoic acid
E
succinic acid
F
acetic acid
G
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; 0.5percent Pd on Rutile TiO2 at 110℃; Product distribution / selectivity; | A 0.77% B 0.38% C 0.24% D 0.05% E 98.28% F 0.02% G 0.26% |
(R)-(+)-1,2-epoxybutane
A
(S)-2-butanol
B
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; 10percentPd/C; 1,2-diaminoethane; mixture of at 25℃; under 37503.8 Torr; for 24h; Conversion of starting material; | A 98.21% B 0.99% |
With hydrogen; 10percentPd/C; 1,2-diaminoethane; mixture of at 25 - 50℃; under 3750.38 - 7500.75 Torr; for 24h; | A 89% B 0.958% |
With hydrogen; palladium 10% on activated carbon In methanol at 25℃; under 3750.38 Torr; for 24h; Conversion of starting material; | A 81.752% B 11.148% |
With hydrogen; carbon; Na2PdCl4; sodium hydroxide; 1,2-diaminoethane; mixture of at 25℃; under 3750.38 Torr; for 24h; Conversion of starting material; | A 71.379% B 0.721% |
With hydrogen; carbon; Na2PdCl4; sodium hydroxide; 1,2-diaminoethane; mixture of In methanol at 25℃; under 3750.38 Torr; for 24h; Conversion of starting material; | A 41.58% B 0.42% |
Conditions | Yield |
---|---|
With 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine cobalt(II) dichloride; diethoxymethylane; sodium triethylborohydride In toluene at -78 - 20℃; for 5h; | 98% |
With hydrogen; ruthenium palladium In propan-1-ol at 89.9℃; Rate constant; | |
With (bis(mesityl-benzimidazol-2-ylidene)phenyl)Co(N2)(PPh3); hydrogen In benzene-d6 at -196.16 - 19.84℃; under 3040.2 Torr; for 2h; | |
With hydrogen In dichloromethane at 20℃; under 3000.3 Torr; for 24h; Time; |
dimethyl cis-but-2-ene-1,4-dioate
A
tetrahydrofuran
B
2-methoxytetrahydrofuran
C
4-butanolide
D
propan-1-ol
E
2-(4'-hydroxybutoxy)-tetrahydrofuran
F
Butane-1,4-diol
G
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; copper catalyst, T 4489, Sud-Chemie AG, Munich at 150 - 280℃; under 187519 Torr; Neat liquid(s) and gas(es)/vapour(s); | A 1% B n/a C 0.4% D n/a E n/a F 98% G 0.5% |
Conditions | Yield |
---|---|
In xylene at reflux 140-106°C for 165 h, then distilling butanol-borane azeotrop; | A 98% B n/a |
catechol butyl borate
N-(salicylidene)aniline N-oxide
B
butan-1-ol
Conditions | Yield |
---|---|
In benzene to benzene soln. of nitrone of salicylaldehyde added (C6H4O2)BOC4H9 (molar ratio 1:1), refluxed for 30 min; concd. in vac., added petroleum ether, ppt. washed with ether, dried, elem. anal.; | A 98% B n/a |
Conditions | Yield |
---|---|
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 15h; Glovebox; Autoclave; | 98% |
With hydrogen at 223.84℃; under 5625.56 Torr; Kinetics; Thermodynamic data; Concentration; Pressure; Temperature; neat (no solvent, gas phase); | |
With [RuH(η2-BH4)(2-di-tert-butylphosphinomethyl-6-diethylaminomethylpyridine)]; hydrogen In tetrahydrofuran at 110℃; under 7600.51 Torr; for 12h; Autoclave; | 97 %Chromat. |
Conditions | Yield |
---|---|
In benzene to benzene soln. of nitrone of salicylaldehyde added (C6H4O2)BOC4H9 (molar ratio 1:1), refluxed for 30 min; concd. in vac., added petroleum ether, ppt. recrystd. from THF/petroleum ether, elem. anal.; | A 97% B n/a |
B
butan-1-ol
Conditions | Yield |
---|---|
In benzene refluxed in benzene for 30 min; | A 96% B n/a |
Conditions | Yield |
---|---|
With 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine cobalt(II) dichloride; diethoxymethylane; sodium triethylborohydride In neat (no solvent) at -78 - 40℃; for 2h; | 96% |
With hydrogen In ethanol at 27℃; under 2250.23 Torr; for 0.416667h; Kinetics; Solvent; Time; Green chemistry; |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 110℃; for 3h; High pressure; | A 96% B n/a |
Conditions | Yield |
---|---|
With crosslinked polystirene anion exchange resin in BH4- form In ethanol for 2h; Ambient temperature; | 95% |
With C54H60N6O6Pd(2+)*2Br(1-); hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene In 1,4-dioxane at 75℃; under 7500.75 Torr; for 6h; | 30% |
bei der elektrolytischen Reduktion; |
catechol butyl borate
α-(2-hydroxy-1-phenyl)-N-methylnitrone
B
butan-1-ol
Conditions | Yield |
---|---|
In benzene to benzene soln. of nitrone of salicylaldehyde added (C6H4O2)BOC4H9 (molar ratio 1:1), refluxed for 30 min; concd. in vac., added petroleum ether, ppt. washed with ether, dried, elem. anal.; | A 95% B n/a |
4-benzyloxycarbonylaminobutyric acid butyl ester
A
4-(benzyloxycarbonylamino)butyric acid
B
butan-1-ol
Conditions | Yield |
---|---|
With methanol; recombinant Bacillus subtilis esterase double mutant E188W/M193C In hexane at 37℃; for 0.5h; pH=7.4; Kinetics; Reagent/catalyst; Time; aq. phosphate buffer; Enzymatic reaction; | A 95% B n/a |
butyl levulinate
A
γ-hydroxy butyl pentanoate
B
5-methyl-dihydro-furan-2-one
C
butan-1-ol
Conditions | Yield |
---|---|
With n-butyl formate; water at 170℃; under 7500.75 Torr; for 6h; Inert atmosphere; chemoselective reaction; | A n/a B 95% C n/a |
benzaldehyde
N-butylamine
acetophenone
A
2,4,6-triphenylpyridine
B
butan-1-ol
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate at 120℃; for 4h; Neat (no solvent); regioselective reaction; | A 95% B 91 %Chromat. |
urethane
methyloxirane
A
4-methyl-2-oxazolidone
B
5-methyl-1,3-oxazolidin-2-one
C
butan-1-ol
Conditions | Yield |
---|---|
With basic molar 1:1 Mg-Fe oxide calcined at 400 °C at 140℃; for 8h; Reagent/catalyst; Temperature; Autoclave; | A n/a B 95% C n/a |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In methanol at 25℃; for 4h; | 94.4% |
1-(t-butyldiphenylsilyloxy)butane
butan-1-ol
Conditions | Yield |
---|---|
With Selectfluor In acetonitrile at 150℃; for 0.166667h; Microwave irradiation; | 94% |
With methanol; trimethylsilyl bromide at 20℃; for 9h; chemoselective reaction; | 90% |
Conditions | Yield |
---|---|
With 2Al(3+)*HO(1-)*5CH3O3S(1-) In dichloromethane at 20℃; for 0.75h; Reagent/catalyst; | 100% |
With ruthenium(III) acetate at 20℃; for 0.5h; | 99% |
With aminosulfonic acid at 15℃; for 3h; | 98% |
Conditions | Yield |
---|---|
With cucurbit[7]uril at 55℃; for 4h; Time; | 100% |
at 20℃; for 4h; | 99% |
With zirconyl(IV) nitrate hydrate at 45℃; for 0.333333h; | 97% |
Conditions | Yield |
---|---|
With diacidic ionic liquid supported on magnetic-silica nanoparticles In neat (no solvent) at 118℃; for 2h; Temperature; Dean-Stark; | 100% |
With sulfuric acid; acetonitrile at 80 - 85℃; for 16 - 18h; | 99% |
With phosphotungstic acid; bis(acetylacetonato)dioxomolybdenum(VI); potassium tetranitroplatinate at 95 - 105℃; under 540.054 Torr; for 1h; | 99.4% |
Conditions | Yield |
---|---|
chlorodi-(n-butyl)tin acetate In chloroform for 0.833333h; Product distribution; Mechanism; Ambient temperature; catalytic activity, various tin(IV) catalysts; | 100% |
chlorodi-(n-butyl)tin acetate In chloroform for 0.833333h; Ambient temperature; | 100% |
With diallyltin(IV)di(2-ethyl hexanoate) In dichloromethane for 0.0833333h; Product distribution; Heating; other alcohols and isocyanates; var. temp. and time; | 93% |
Conditions | Yield |
---|---|
With crosslinked sulphonated polystyrene at 80℃; for 2h; Product distribution; other acids and solvents; var. catalysts, temp. and time; | 100% |
zirconium(IV) oxide for 2h; Heating; | 100% |
phosphomolybdic acid hydrate at 65 - 70℃; for 1h; Product distribution; Further Variations:; Catalysts; Reaction partners; | 100% |
Conditions | Yield |
---|---|
Stage #1: butan-1-ol With triethylamine In dichloromethane at 25℃; Stage #2: methanesulfonyl chloride In dichloromethane at 0 - 20℃; | 100% |
With triethylamine In dichloromethane at -15℃; for 1h; Green chemistry; | 100% |
With sodium hydroxide; potassium carbonate; tetra(n-butyl)ammonium hydrogensulfate In benzene at 15 - 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
Stage #1: butan-1-ol With RuCpCl(o-EtOdppe); silver(I) 4-methylbenzenesulfonate In toluene for 0.0833333h; Inert atmosphere; Stage #2: allyl alcohol In toluene at 100℃; for 2h; Inert atmosphere; regioselective reaction; | 100% |
With boron fluoride ether; mercury(II) diacetate; benzene | |
With ammonium chloride; copper; copper(l) chloride Reagens 4: wss. Salzsaeure; |
Conditions | Yield |
---|---|
With [Al(H2O)6][MS]3 In cyclohexane for 1h; Reagent/catalyst; Dean-Stark; Reflux; | 100% |
With Candida antarctica B lipase In 2,2,4-trimethylpentane at 40℃; for 3h; Enzymatic reaction; | 98% |
With DOOl-AlCl3 superacid resin for 1.5h; Heating; | 97% |
Conditions | Yield |
---|---|
With 3,3′-(2,2-bis(hydroxymethyl)propane-1,3-diyl)bis(1-methyl-1H-imidazol-3-ium) hydrogen sulfate for 2h; Dean-Stark; Reflux; | 100% |
With [3-(1-methylimidazolium-3-yl)propane-1-sulfonate]3PW12O40 at 130℃; for 3h; | 98.6% |
With Candida antarctica lipase B In cyclohexane at 45℃; for 3h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; | 92% |
Conditions | Yield |
---|---|
With N-nitro-2,4,6-trimethylpyridinium tetrafluoroborate In acetonitrile at 0℃; for 2h; | 100% |
With carbon dioxide; dinitrogen pentoxide at 0℃; under 45004.5 - 60006 Torr; for 0.5h; Autoclave; | 94% |
With nitric acid; urea; europium(III) trifluoromethanesulfonate In cyclohexane at 80℃; for 10h; Schlenk technique; | 90% |
Conditions | Yield |
---|---|
With boric acid In toluene Reflux; | 100% |
With aluminum oxide; sodium borate; carbon dioxide at 80℃; under 1034.32 Torr; for 4h; | 38% |
With boron trichloride; pentane |
Conditions | Yield |
---|---|
With oxygen; phosphan; copper dichloride at 24.9℃; Rate constant; Product distribution; other acohols and reagents, var. concentration of reagents and temperatures; | 100% |
With oxygen; phosphan; copper dichloride at 24.9℃; | 100% |
With oxygen; copper dichloride at 59.9℃; | 100% |
Conditions | Yield |
---|---|
With C29H44Cl2N2Ru; potassium tert-butylate In toluene for 15h; Reagent/catalyst; Time; Reflux; | 100% |
Ru complex at 118℃; for 12h; Inert atmosphere; | 99% |
With dihydrogen peroxide; bromine In dichloromethane; water at 20℃; for 2h; | 99% |
Conditions | Yield |
---|---|
With oxidase In water at 40℃; for 1.5h; Reformatsky Reaction; Enzymatic reaction; | 100% |
With tetramethylammonium monofluorochromate(VI) In dichloromethane at 20℃; for 2h; | 98% |
With DIQCC In dichloromethane at 20℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; sodium trimethylsilylpropionate-d4; C18H22N4O2Ru(2+)*2F6P(1-); water at 20℃; for 0.5h; | 100% |
With oxygen In water at 80℃; under 760.051 Torr; for 24h; | 99.7% |
With potassium hydroxide at 50℃; electrolysis; | 98.8% |
Conditions | Yield |
---|---|
With tetrachloromethane; bis(acetylacetonate)oxovanadium; triethylamine at 175℃; for 5h; Inert atmosphere; Autoclave; | 100% |
With sodium hydroxide; 1,5-bis-(N-benzyl-N,N-diethylammonium)diethylether dichloride at 50 - 60℃; for 4h; | 90% |
With potassium hydroxide; tetrabutylammomium bromide; potassium carbonate at 122℃; for 0.0152778h; | 86% |
Conditions | Yield |
---|---|
With 1-chloro-3-hydroxy-1,1,3,3-tetrabutyldistannoxane at 120℃; for 24h; Esterification; | 100% |
Zn4O (OCOCF3)6(CF3COOH)n In di-isopropyl ether for 18h; Product distribution / selectivity; Inert atmosphere; Reflux; | 100% |
With di-tert-butyl dicarbonate; magnesium chloride at 20℃; | 97% |
Conditions | Yield |
---|---|
With Amano P at 25℃; for 6h; | 100% |
In toluene at 90℃; Inert atmosphere; | 90% |
at 127℃; for 2h; | 85% |
Conditions | Yield |
---|---|
With Amano P at 25℃; for 6h; | 100% |
Heating; |
1,4-diisocyanatobenzene
butan-1-ol
(4-Butoxycarbonylamino-phenyl)-carbamic acid butyl ester
Conditions | Yield |
---|---|
for 4h; Heating; | 100% |
N,N'-dibenzyl-2,3,5,6-piperazinetetraone
butan-1-ol
1,3-Dibenzyl-2-hydroxy-4,5-dioxo-imidazolidine-2-carboxylic acid butyl ester
Conditions | Yield |
---|---|
for 6h; Heating; | 100% |
Conditions | Yield |
---|---|
for 24h; | 100% |
With sulfuric acid for 16h; Heating; | 78% |
1,3-Phenylene diisocyanate
butan-1-ol
(3-Butoxycarbonylamino-phenyl)-carbamic acid butyl ester
Conditions | Yield |
---|---|
for 4h; Heating; | 100% |
di(4-isocyanatophenyl)methane
butan-1-ol
dibutyl diphenyl methane-4,4’-dicarbamate
Conditions | Yield |
---|---|
for 4h; Heating; | 100% |
In tetrahydrofuran at 20℃; for 2h; | 84% |
ethyl 2-hydroxypyrrolidine-1-carboxylate
butan-1-ol
2-Butoxy-pyrrolidine-1-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With acetic acid | 100% |
sec-Butyl acetate
butan-1-ol
A
acetic acid butyl ester
B
iso-butanol
Conditions | Yield |
---|---|
With water; sodium butanolate at 30℃; for 0.0833333h; carried out in a reaction-distillation unit, industrial preparation; | A n/a B 100% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 25℃; for 24h; | 100% |
With hydrogenchloride Heating; | |
With chloro-trimethyl-silane at 25℃; for 24h; |
3-(2-vinyloxyethoxy)-1,2-propylene carbonate
butan-1-ol
4-[2-(1-Butoxy-ethoxy)-ethoxymethyl]-[1,3]dioxolan-2-one
Conditions | Yield |
---|---|
With heptafluorobutyric Acid at 20 - 45℃; for 0.333333h; | 100% |
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