DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:110-74-7
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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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:110-74-7
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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:110-74-7
Min.Order:10 Gram
FOB Price: $100.0
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
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:110-74-7
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
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HuBei ipure is a diversified product production and operation enterprise, with API, pharma intermediates, and other fine chemicals as well as R&D and pigments development and sales as one of the large enterprises, with more than 130 acres of pl
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
Formic acid, propylester Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Supply top quality products with a reasonable price Application:api
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
high purity Application:Drug intermediates Materials intermediates and active molecules
Conditions | Yield |
---|---|
With oxygen; toluene-4-sulfonic acid; acetic acid at 20℃; for 2h; Baeyer-Villiger Ketone Oxidation; | 97% |
propan-1-ol
sodium salt of β-mercaptonaphthalene
A
propyl methanoate
B
naphthalene-2-yl(propyl)sulfane
Conditions | Yield |
---|---|
With carbon monoxide at 150℃; under 75006 Torr; for 10h; | A n/a B 95% |
Conditions | Yield |
---|---|
With pyridine; N,N'-dibromo-N,N'-(1,2-ethanediyl)bis(p-toluenesulfonamide); triphenylphosphine In dichloromethane at 20℃; | 91% |
With sulfuric acid In water for 4h; Reflux; | 75% |
With sulfuric acid In 1,4-dioxane at 60℃; Equilibrium constant; |
propan-1-ol
D-Fructose
A
5-(n-propoxymethyl)-2-furancarboxadehyde
B
Dipropyl ether
C
propyl methanoate
D
n-propyl levulinate
Conditions | Yield |
---|---|
With poly(p-styrenesulfonic acid)-grafted carbon nanotubes at 120℃; for 24h; Sealed tube; Green chemistry; chemoselective reaction; | A n/a B n/a C n/a D 86% |
Conditions | Yield |
---|---|
With Cu/Al2O3; dihydrogen peroxide In chloroform at 80℃; for 24h; | 83% |
propan-1-ol
phenylacetylene
A
propyl methanoate
B
propyl benzoate
Conditions | Yield |
---|---|
With bis-[(trifluoroacetoxy)iodo]benzene at 60℃; for 15h; Sealed tube; | A n/a B 72% |
5,10,15,20-tetra(2,4,6-trimethylphenyl)porphyrinate rhodium(II)
Dipropyl ether
(5,10,15,20-tetra(2,4,6-trimethylphenyl)porphyrinato)rhodium(III) ethyl
B
propyl methanoate
Conditions | Yield |
---|---|
With water; tetraphenylphosphonium bromide; triphenylphosphine; potassium hydroxide at 25℃; Inert atmosphere; Darkness; regioselective reaction; | A 62% B n/a |
2-(tert-butylperoxy)tetrahydrofuran
A
4-butanolide
B
propyl methanoate
D
acetone
E
tert-butyl alcohol
Conditions | Yield |
---|---|
In various solvent(s) at 120℃; for 14h; Mechanism; Product distribution; | A 30% B 11% C 12% D 7% E 61% |
propan-1-ol
D-glucose
A
formic acid
B
propyl methanoate
C
1-Propyl acetate
D
carbon dioxide
E
carbon monoxide
F
acetic acid
Conditions | Yield |
---|---|
With H8[PMo7V5O40]; oxygen In water at 90℃; under 15001.5 Torr; for 24h; Autoclave; | A n/a B n/a C n/a D 24% E 21% F n/a |
tripropyl orthoformate
benzoyl chloride
A
1-Chloropropane
B
propyl methanoate
C
propyl benzoate
tripropyl orthoformate
acetaldehyde
A
acetaldehyde dipropyl acetal
B
propyl methanoate
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
In water Product distribution; Mechanism; Irradiation; γ irradiation; |
1,3-dioxane
A
propan-1-ol
B
formaldehyd
C
1,3-dioxine
D
ethene
E
propyl methanoate
F
allyl alcohol
Conditions | Yield |
---|---|
Mechanism; Product distribution; Quantum yield; Heating; 185 nm vacuum-ultraviolet photolysis; |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 120℃; Product distribution; Rate constant; other temperature, various concentrations of peroxide, in the presence of ethyl orthoformate; | |
With di-tert-butyl peroxide at 120℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
dipropoxymethane
tris(ethylsulfanyl)methane
A
bis(ethylthio)methane
B
ethyl propyl sulfide
C
propyl methanoate
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In various solvent(s) at 30℃; Product distribution; equilibrium concentrations; various temperature and reactant ratios, other catalysts; |
Conditions | Yield |
---|---|
With ozone In tetrachloromethane at 25℃; Rate constant; k= 0.7 liter/mole.sec; | |
With ozone In tetrachloromethane at 18℃; Rate constant; Mechanism; |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 130℃; Rate constant; kinetic isotope effect; further temperatures; |
tripropyl orthoformate
A
propane
B
propyl methanoate
C
Dipropyl carbonate
D
propionaldehyde
Conditions | Yield |
---|---|
With di-tert-butyl peroxide In chlorobenzene at 140℃; for 4h; Kinetics; Mechanism; Product distribution; various temperatures, rates of formation; |
carbon monoxide
A
ethanol
B
Methyl formate
C
propyl methanoate
D
ethylene glycol
Conditions | Yield |
---|---|
With 2-hydroxypyridin; hydrogen; acetylacetonatodicarbonylrhodium(l) In various solvent(s) at 230℃; under 1499480 Torr; for 4.5h; Further byproducts given. Title compound not separated from byproducts; | A 191 mmol B 52 mmol C 29 mmol D 1000 mmol |
1,3-Bis(1,3-dioxan-2-yloxy)propane
A
trimethylene carbonate
B
propyl methanoate
C
2-propoxy-1,3-dioxane
D
3-([1,3]Dioxan-2-yloxy)-propionaldehyde
E
propyl 3-(1,3-dioxan-2-yloxy)propyl carbonate
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 130℃; for 0.5h; Product distribution; | A 0.02 mol B 0.01 mol C 0.02 mol D 0.01 mol E 0.06 mol |
2-propoxy-1,3-dioxane
A
trimethylene carbonate
B
propane
C
propyl methanoate
D
Dipropyl carbonate
E
propionaldehyde
Conditions | Yield |
---|---|
With di-tert-butyl peroxide In chlorobenzene at 130℃; Product distribution; Rate constant; Mechanism; |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 140℃; for 3h; conversion, concentration of products; |
2-propoxyethanol
A
2-ethyl-1,3-dioxolane
B
propyl methanoate
C
n-propoxyacetaldehyde
Conditions | Yield |
---|---|
With hydroxide at 23.85℃; under 760 Torr; Rate constant; Product distribution; Mechanism; | A 5.4 % Chromat. B 47 % Chromat. C 15 % Chromat. |
Conditions | Yield |
---|---|
Geschwindigkeit der Umsetzung; |
Dipropyl ether
A
propyl propionate
B
propyl methanoate
C
acetaldehyde
D
propionaldehyde
Conditions | Yield |
---|---|
With nitric oxide Kinetics; Oxidation; UV-irradiation; |
Conditions | Yield |
---|---|
With hydrogen; triethylamine; TpRu(PPh3)(CH3CN)H at 100℃; under 38000 Torr; for 16h; |
Conditions | Yield |
---|---|
With hydrogen; potassium carbonate at 169.84℃; under 22502.3 Torr; for 2h; |
Conditions | Yield |
---|---|
Conversion of starting material; |
Conditions | Yield |
---|---|
With oxygen; [Ru(CO)2Cp]2 under 375.038 Torr; for 168h; |
Conditions | Yield |
---|---|
With Cp*2Sm(THF)2 In toluene Ambient temperature; further reagent: SmI2; | 99% |
Conditions | Yield |
---|---|
With Cp*2Sm(THF)2 In toluene Ambient temperature; | 99% |
propyl methanoate
Conditions | Yield |
---|---|
Stage #1: (S)-2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-ethyl ester With sodium t-butanolate In tetrahydrofuran at -70℃; for 3h; Inert atmosphere; Stage #2: propyl methanoate In tetrahydrofuran at -70℃; for 5h; Stage #3: With trifluoroacetic acid In dichloromethane at 5 - 25℃; for 4h; | 95.7% |
Conditions | Yield |
---|---|
With magnesium; lithium chloride In tetrahydrofuran; dichloromethane at 20 - 67℃; for 1.5h; Time; | 91.1% |
propyl methanoate
1-(Aminomethyl)isoquinoline dihydrochloride
2-formamidomethylisoquinoline
Conditions | Yield |
---|---|
With TEA In ethanol for 2h; Heating; | 89% |
propyl methanoate
p-trifluoromethylphenyl bromide
1-propyl 4-(trifluoromethyl)benzoate
Conditions | Yield |
---|---|
Stage #1: p-trifluoromethylphenyl bromide With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: propyl methanoate In tetrahydrofuran; hexane at -78℃; for 3h; Stage #3: With propan-1-ol; iodine; potassium carbonate In tetrahydrofuran; hexane at -78 - 20℃; for 14h; | 86% |
propyl methanoate
2,2-diethoxy-ethanamine
2,2-diethoxy-1-formylaminoethane
Conditions | Yield |
---|---|
for 3h; Reflux; | 86% |
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride hexahydrate In hexane; water at 80℃; for 14h; | 86% |
Adipic acid
propyl methanoate
A
Hexanedioic acid monopropyl ester
B
di-n-propyl adipate
Conditions | Yield |
---|---|
With Dowex 50W-X2 (50-100 mesh) In octane at 70℃; for 2.66667h; | A 85% B 6% |
With Dowex 50Wx2 In octane at 70℃; for 2.66667h; Esterification; | A 85% B 6% |
propyl methanoate
quinolin-2-ylmethanamine bischlorohydrate
N-(2-Quinolylmethyl)formamide
Conditions | Yield |
---|---|
With TEA In ethanol for 2h; Heating; | 83% |
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; copper(II) bis(trifluoromethanesulfonate) In 1,2-dichloro-ethane at 130℃; for 12h; Sealed tube; | 82% |
Conditions | Yield |
---|---|
With Cp*2Sm(THF)2 In toluene Ambient temperature; | 80% |
Conditions | Yield |
---|---|
at 115℃; for 2h; | 80% |
Conditions | Yield |
---|---|
With N-methyl-N-phenylformamide at 60℃; for 9h; | 76% |
propyl methanoate
3-formamidomethylisoquinoline
Conditions | Yield |
---|---|
With TEA In ethanol for 2h; Heating; | 75% |
Conditions | Yield |
---|---|
Stage #1: deoxyvasicinone; propyl methanoate With sodium at 0 - 20℃; Stage #2: With water Cooling with ice; | 75% |
propyl methanoate
2-(Aminomethyl)-4-methoxyquinoline dihydrochloride
<(4-Methoxy-2-quinolyl)methyl>formamide
Conditions | Yield |
---|---|
With TEA In ethanol for 2h; Heating; | 74% |
propyl methanoate
dichloromethyl propyl ether
Conditions | Yield |
---|---|
With oxalyl dichloride; N-methyl-N-phenylformamide at 60℃; for 17h; | 74% |
With oxalyl dichloride; N-methyl-N-phenylformamide |
propyl methanoate
Conditions | Yield |
---|---|
for 24h; Inert atmosphere; Reflux; | 73% |
Conditions | Yield |
---|---|
With tris(2,2'-bipyridyl)ruthenium dichloride; trimethylsilyl cyanide; 4-cyano-1-isopropoxypyridin-1-ium trifluoromethanesulfonate at 20℃; for 12h; Schlenk technique; Inert atmosphere; Irradiation; | 72% |
propyl methanoate
Conditions | Yield |
---|---|
With potassium carbonate for 21h; Inert atmosphere; Reflux; | 68% |
propyl methanoate
Conditions | Yield |
---|---|
With potassium carbonate for 41h; Inert atmosphere; Reflux; | 68% |
Conditions | Yield |
---|---|
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h; | 67% |
dimethylacetylene
propyl methanoate
(2E,5E)-3,5-dimethylhepta-2,5-dien-4-ol
Conditions | Yield |
---|---|
With isobutylmagnesium bromide; titanocene dichloride | 65% |
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