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:75-30-9
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Type:Lab/Research institutions
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Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryProduct name 2-Iodopropane CAS 75-30-9 Synonyms 2-Iodopropane CAS 75-30-9 CAS NO. 75-30-9 Molecular Form
Cas:75-30-9
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inquiryOur 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:75-30-9
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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
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
Cas:75-30-9
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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
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:75-30-9
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inquiryProduct name: 2-Iodopropane CAS No.:75-30-9 Molecule Formula:C3H7I Molecule Weight:169.99 Purity: 98% Package: 25kg/drum Description:Colorless or slightly yellow transpanrent liquid Manufacture Standards:Enterprise Standard
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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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 qualityAppearance:white crystalline powder 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 a comprehensive enterprise, is located in High-Tech Science Park,Changsha,Chia . Specializing in R&D, manufacture and marketing, we provide a wide range of products and the most professional services to meet the
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:75-30-9
Min.Order:1 Kilogram
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Type:Trading Company
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in storeAppearance:Colorless to light yellow transparent liquid Package:500g Application:Organic Chemicals
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Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiry2-Iodopropane Basic information Product Name: 2-Iodopropane Synonyms: 2-iodo-propan;2-Jodpropan;2-propyliodide;2-Propyljodid;i-Propyl iodide;iso-C3H7I;Isopropyl iodine;Is
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryShanghai AngewChemCo., Ltd. is an innovative enterprise on fine chemicals and pharmaceuticals. Based on Shanghai R&D center and Hunan chemical manufacturing plant, we offer chemical research, process development, and large-scale production. Com
Why Choose Us: 1.Own chemical factory 2.Abundant professional production experience 3.Sample is free of charge and in stock with fast delivery 4.Price,quality&service,we care that all your cares 5.Prompt reply keep in touch to sa
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryProfile HeBei Ruishun Trade Co.LTD, registered capital one million,have a production of pharmaceutical raw materials, pharmaceutical raw materials factory reagent r&d center,Seek development by credit
BaiFuChem is a Professional chemical raw material supplier in China, our main products include Biochemical , Pharma Intermediate and Organic chemical etc. BaiFuChem have wealth of products,experience , expertise and state-of-the-art
Conditions | Yield |
---|---|
With iodoform; sodium iodide In N,N-dimethyl-formamide for 3h; Catalytic behavior; Irradiation; | 91% |
With acetyl iodide at 80 - 90℃; for 1.5h; | 24% |
With iodine; aluminium |
(i-C3H7)3SbI2
A
2-iodo-propane
B
tri(isopropyl)antimony
C
diisopropylantimony iodide
Conditions | Yield |
---|---|
under Ar, decomposed at 135°C for 30 min; distd., not separated from triisopropyl stibine; elem. anal.; | A 89% B n/a C n/a |
Conditions | Yield |
---|---|
With 2-fluoro-2-(piperidin-1-yl)-4-(2,3,5,6-tetrafluoropyridin-4-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiole In 1,4-dioxane at 45℃; for 14h; Schlenk technique; Inert atmosphere; | 74% |
Conditions | Yield |
---|---|
With N-iodo-succinimide In chlorobenzene for 3h; Irradiation; | A 51% B 18% |
Conditions | Yield |
---|---|
With CCl4*2AlI3 In dichloromethane at -20℃; for 1.5h; | 50% |
5'-O-(4,4'-dimethoxytrityl)-2-N-<2-<(tert-butyldiphenylsilyloxy)methyl>benzoyl>guanosine
tert-butyldimethylsilyl chloride
A
2-iodo-propane
B
5'-O-(4,4'-dimethoxytrityl)-3'-O-(tert-butyldimethylsilyl)-2-N-<2-<(tert-butyldiphenylsilyloxy)methyl>benzoyl>guanosine
Conditions | Yield |
---|---|
With pyridine; silver nitrate In tetrahydrofuran | A 42% B 16% |
Conditions | Yield |
---|---|
With water; hydrogen iodide |
propene
2-iodo-propane
Conditions | Yield |
---|---|
With hydrogen iodide | |
With ascaridole; hydrogen iodide | |
With hydrogen iodide; diphenylamine | |
With hydrogen iodide |
Conditions | Yield |
---|---|
With hydrogen iodide; diphenylamine |
Conditions | Yield |
---|---|
With hydrogen iodide |
1,2-iodochloropropane
2-iodo-propane
Conditions | Yield |
---|---|
With hydrogen iodide |
Conditions | Yield |
---|---|
With phosphoric acid; potassium iodide | |
With diiodosilane In chloroform-d1 Ambient temperature; relative rates, other reagents, var. ethers; |
Conditions | Yield |
---|---|
With water; potassium iodide |
Conditions | Yield |
---|---|
mit UV-Licht (253.7 nm),in fluess. Zustand;bei Abwesenheit von Sauerstoff.Irradiation; |
Conditions | Yield |
---|---|
With phosphorus; water; iodine und nachfolgendes Dastillieren des Reaktionsprodukts; | |
With water; hydrogen iodide | |
With phosphorous; water; iodine | |
With hydrogen iodide In water; benzene at 100℃; under 15514.9 Torr; for 16h; Inert atmosphere; Autoclave; | 100 %Chromat. |
Conditions | Yield |
---|---|
With pyridine; tributyltin iodide at 125℃; Thermodynamic data; Equilibrium constant; Δ G; | |
With sodium iodide In acetone at 55℃; Kinetics; quantitative reaction kinetics in liquid state by in situ X-ray absorption fine structure spectroscopy; | |
With acetone; sodium iodide |
triisopropyl phosphite
methyl iodide
A
2-iodo-propane
B
diisopropyl methanephosphonate
Conditions | Yield |
---|---|
reagiert analog mit Brom-diphenyl-p-biphenylyl-methan und Homologen; |
Conditions | Yield |
---|---|
With diiodosilane In chloroform-d1 at 22℃; for 4h; | 99 % Spectr. |
allyl iodid
Chloroiodomethane
isopropylmagnesium chloride
A
2-iodo-propane
B
Isobutyl iodide
C
4-iodobut-1-ene
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether at -40℃; for 4.5h; Product distribution; | |
In tetrahydrofuran at -40℃; for 4.5h; |
diisopropyl ethylphosphonite
1,1,1,2,2,3,3-heptafluoro-3-iodo-propane
A
2-iodo-propane
B
isopropyl ethyl(heptafluoropropyl)phosphinate
Conditions | Yield |
---|---|
In octane Rate constant; Kinetics; Thermodynamic data; E (activ.); ΔH(excit.); ΔS(excit.); ΔG(excit.); |
propene
acetic acid
A
2-iodo-propane
B
Isopropyl acetate
C
isopropyl alcohol
Conditions | Yield |
---|---|
With carbon monoxide; water; hydrogen iodide; TsVK-2; palladium at 110℃; under 60800 Torr; for 2h; Product distribution; further temperature (130 deg C); |
Conditions | Yield |
---|---|
With diiodosilane; iodine 1.) CDCl3, 22 deg C, 10 min, 2.) 30 min; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With diiodosilane; iodine In chloroform-d1 at 22℃; for 3h; | 100 % Spectr. |
Conditions | Yield |
---|---|
With diiodosilane In chloroform-d1 for 0.166667h; Ambient temperature; other reaction time: 80 min, effect of iodine; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
propene
carbon monoxide
isobutyric Acid
A
2-iodo-propane
B
isopropyl isobutyrate
C
isopropyl butyrate
D
isopropyl alcohol
E
butyric acid
Conditions | Yield |
---|---|
With water; hydrogen iodide; TsVK-2; palladium at 130℃; under 60800 Torr; for 2h; Product distribution; further temperature (110, 150, 170, 200 deg C); effect of the concentration of HI; effect of the pressure of CO; |
isopropyl radical
methyl iodide
A
2-iodo-propane
B
methyl radical
Conditions | Yield |
---|---|
Equilibrium constant; |
phenol
A
2-iodo-propane
B
tetrachloromethane
C
phenoxy radical
Conditions | Yield |
---|---|
In tetrachloromethane at 22℃; Rate constant; multistep reaction; |
Conditions | Yield |
---|---|
With trimethylsilyl iodide; bismuth(III) iodide In neat (no solvent) at 80℃; for 0.25h; | 98 % Chromat. |
N-methylcyclohexylamine
2-iodo-propane
1-isopropyl-1-methyl-piperidinium; iodide
Conditions | Yield |
---|---|
In chloroform at 60℃; for 8h; | 100% |
In chloroform Heating; |
2-iodo-propane
3-methylenebicyclo[2.2.1]heptan-2-one
3-isobutylbicyclo<2.2.1>heptan-2-one
Conditions | Yield |
---|---|
With copper(l) iodide; zinc In water Product distribution; further solvent: aq. ethanol, further activators: ammonium formate, ammonium chloride; ultrasonic irradiation; | 100% |
With copper(l) iodide; zinc In water ultrasonic irradiation; | 100% |
2-iodo-propane
5-hydroxynaphtho-1,4-quinone
5-isopropoxy-1,4-naphthoquinone
Conditions | Yield |
---|---|
With silver(l) oxide In dichloromethane at 20℃; for 20h; Green chemistry; regioselective reaction; | 100% |
With silver(l) oxide In chloroform for 0.333333h; Ambient temperature; | 77% |
2-iodo-propane
Conditions | Yield |
---|---|
In acetonitrile for 43h; | 100% |
2-iodo-propane
3-(4-hydroxy-2-nitrophenyl)pyridine
3-(4-isopropoxy-2-nitrophenyl)pyridine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 40℃; for 6h; | 100% |
Conditions | Yield |
---|---|
With sodium azide; [bis(acetoxy)iodo]benzene; trifluoroacetic acid In isopropyl alcohol Product distribution; various solvents; | 100% |
With sodium azide; [bis(acetoxy)iodo]benzene; trifluoroacetic acid In isopropyl alcohol Heating; | 100% |
With tert.-butylhydroperoxide; acetic acid ; ferriacetate; trifluoroacetic acid In acetic acid for 4h; Heating; | 92% |
2-iodo-propane
benzeneacetic acid methyl ester
2-phenyl-3-methylbutyric acid methyl ester
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide In tetrahydrofuran at -78℃; | 100% |
With 2-pyrrolidinon In N,N-dimethyl-formamide Flow reactor; | 16% |
With 1) EGB.2 1) -78 deg C, 2) -78 deg C, 15 min; Yield given. Multistep reaction; |
2-iodo-propane
3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-2,6-diethyl-7-hydroxy-chromen-4-one
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 34.5h; Heating; | 100% |
With potassium carbonate In acetone Heating; | 99.8% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; | 100% |
2-iodo-propane
2-[(E)-2-nitroethenyl]furan
(E)-1-(2-furyl)-3-methyl-1-butene
Conditions | Yield |
---|---|
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h; | 100% |
With air; triethyl borane In tetrahydrofuran at 20℃; | 100% |
Conditions | Yield |
---|---|
With air; triethyl borane In tetrahydrofuran at 20℃; | 100% |
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h; | 98% |
2-iodo-propane
(E)-1-methoxy-4-(2-nitrovinyl)benzene
(E)-1-methoxy-4-(3-methyl-but-1-en-1-yl)benzene
Conditions | Yield |
---|---|
With triethyl borane; oxygen In tetrahydrofuran at 20℃; | 100% |
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h; | 99% |
With triethyl borane In diethyl ether; water | |
With triethyl borane In tetrahydrofuran at 20℃; |
2-iodo-propane
1-nitro-2-(4-chlorophenyl)ethylene
Conditions | Yield |
---|---|
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h; | 100% |
With air; triethyl borane In tetrahydrofuran at 20℃; | 98% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In benzene at 80℃; for 4h; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; water; sodium chloride In acetonitrile for 20h; pH=2; Solvent; pH-value; Electrochemical reaction; Green chemistry; | 100% |
With 2,2'-azobis(isobutyronitrile); tert-butyl(2,6-dimethoxy-1-methylcyclohexa-2,5-dien-1-yl)dimethylsilane In hexane for 14h; Giese-type addition; Heating; | 89% |
With indium In methanol; water at 20℃; for 0.5h; | 86% |
2-iodo-propane
Conditions | Yield |
---|---|
With triethyl borane; tri-n-butyl-tin hydride; magnesium bromide In hexane; dichloromethane at 0℃; for 1h; | 100% |
2-iodo-propane
4-(7-hydroxy-6-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester
4-(7-isopropoxy-6-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 100% |
2-iodo-propane
3-hydroxy-4-aminobenzoic acid methyl ester
4-amino-3-isopropoxybenzoic acid methyl ester
Conditions | Yield |
---|---|
With caesium carbonate In acetone at 60℃; for 2h; Inert atmosphere; | 100% |
With caesium carbonate In acetone for 10h; Heating; | 90% |
With caesium carbonate In acetone for 10h; Heating / reflux; | 90% |
With caesium carbonate In acetone at 120℃; for 1h; Microwave; | 60% |
With caesium carbonate In acetone |
2-iodo-propane
1-triphenylphosphoranylidene-2-propanone
4-methyl-1-(triphenylphosphaneylidene)pentan-2-one
Conditions | Yield |
---|---|
Stage #1: 1-triphenylphosphoranylidene-2-propanone With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at -78 - 20℃; | 100% |
2-iodo-propane
4-tert-butylbenzyl mercaptan
Conditions | Yield |
---|---|
Stage #1: 4-tert-butylbenzyl mercaptan With tetra-(n-butyl)ammonium iodide; caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 2-iodo-propane In N,N-dimethyl-formamide at 0 - 20℃; for 18h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 9H-fluorene With n-butyllithium In tetrahydrofuran; hexane at 20℃; for 1.5h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at 20℃; for 2h; Further stages.; | 100% |
Stage #1: 9H-fluorene With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -15℃; for 0.333333h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at -15℃; for 0.5h; Further stages.; | |
With lithium diisopropyl amide In tetrahydrofuran at -10℃; |
2-iodo-propane
5,6-bis(4-methoxyphenyl)-2H-pyridazin-3-one
Conditions | Yield |
---|---|
100% |
1,1-dimethylethyl 4-(4'-pyridinyloxy)-1-piperidinecarboxylate
2-iodo-propane
4-[(1-{tert-butoxycarbonyl}-4-piperidinyl)oxy]-1-(1-methylethyl)pyridinium iodide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
In dichloromethane at 90℃; for 2.5 - 48h; |
2-iodo-propane
methyl 3-cyano-4-hydroxybenzoate
3-cyano-4-isopropoxybenzoic acid methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 50℃; for 16h; | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 16h; | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 12h; Inert atmosphere; |
2-iodo-propane
4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
4-chloro-5-iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
Stage #1: 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 0.05h; Stage #2: 2-iodo-propane | 100% |
In N,N-dimethyl-formamide |
2-iodo-propane
5-(1-methyl-6-trifluoromethyl-2(1H)-pyridon-3-yl)-2-chloro-4-fluorobenzoic acid
isopropyl 5-(1-methyl-6-trifluoromethyl-2(1H)-pyridon-3-yl)-2-chloro-4-fluorobenzoate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide | 100% |
2-iodo-propane
tert-butyl 6-bromopyridin-2-ylcarbamate
tert-butyl N-(6-bromo-2-pyridyl)-N-isopropylcarbamate
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 25.5h; | 100% |
2-iodo-propane
7-benzyloxy-6-bromo-2-isopropylaminoquinazoline
Conditions | Yield |
---|---|
Stage #1: 7-benzyloxy-6-bromo-2-aminoquinazoline With sodium hydride In N,N-dimethyl-formamide at 5℃; for 0.5h; Stage #2: 2-iodo-propane In N,N-dimethyl-formamide at 60℃; for 1.5h; Stage #3: 2-iodo-propane With sodium hydride Product distribution / selectivity; more than 3 stages; | 100% |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 byproducts: I(1-); react. in a glove box under Ar at 20°C, addn. of the organic halide via syringe to a soln. of Cp3UiPr(1-) in THF-d8, react. time: 10 min; determination by 1H NMR spectroscopy; | 100% |
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