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Dayang Chem (Hangzhou) Co.,Ltd.

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

Propyl formate

Cas:110-74-7

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

inquiry

Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

Propyl formate

Cas:110-74-7

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

inquiry

Hangzhou Keyingchem Co.,Ltd

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

Propyl formate

Cas:110-74-7

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou J&H Chemical Co., Ltd.

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

Formic acid, propylester

Cas:110-74-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Zibo Hangyu Biotechnology Development Co., Ltd

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

High Purity n-propyl formate

Cas:110-74-7

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

inquiry

Henan Allgreen Chemical Co.,Ltd

high 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

Propyl ForMate

Cas:110-74-7

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Henan Tianfu Chemical Co., Ltd.

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.

Formic acid, propylester

Cas:110-74-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

factory supply CAS 110-74-7 with competitive price

Cas:110-74-7

Min.Order:1 Kilogram

FOB Price: $112.0

Type:Trading Company

inquiry

Antimex Chemical Limied

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

Formic acid, propylester

Cas:110-74-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

HENAN SUNLAKE ENTERPRISE CORPORATION

Henan Sunlake Enterprise Corporation Our Advantages 1, Any inquiry about ch

PROPYL FORMATE 110-74-7

Cas:110-74-7

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

HuBei Ipure Biotech CO.,ltd

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

PROPYL FORMATE

Cas:110-74-7

Min.Order:1 Gram

FOB Price: $1.0 / 2.0

Type:Trading Company

inquiry

Hangzhou Share Chemical Co., Ltd

At Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi

n-Propyl forMate

Cas:110-74-7

Min.Order:1 Gram

Negotiable

Type:Other

inquiry

Shanghai united Scientific Co.,Ltd.

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

Formic acid, propylester

Cas:110-74-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Run-Biotech Co., Ltd.

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

PROPYL FORMATE

Cas:110-74-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Nanjing Raymon Biotech Co., Ltd.

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

Formic acid, propylester

Cas:110-74-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Hebei Ruishun Trade Co.,Ltd

Supply top quality products with a reasonable price Application:api

110-74-7

Cas:110-74-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Debye Scientific

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

Propylformate

Cas:110-74-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Changzhou Foreign Trade Corp

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

propyl formate

Cas:110-74-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

NovaChemistry

high purity Application:Drug intermediates Materials intermediates and active molecules

PROPYL FORMATE

Cas:110-74-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

butyraldehyde
123-72-8

butyraldehyde

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With oxygen; toluene-4-sulfonic acid; acetic acid at 20℃; for 2h; Baeyer-Villiger Ketone Oxidation;97%
propan-1-ol
71-23-8

propan-1-ol

sodium salt of β-mercaptonaphthalene
39689-37-7

sodium salt of β-mercaptonaphthalene

A

propyl methanoate
110-74-7

propyl methanoate

B

naphthalene-2-yl(propyl)sulfane
75052-54-9

naphthalene-2-yl(propyl)sulfane

Conditions
ConditionsYield
With carbon monoxide at 150℃; under 75006 Torr; for 10h;A n/a
B 95%
propan-1-ol
71-23-8

propan-1-ol

formic acid
64-18-6

formic acid

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
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
71-23-8

propan-1-ol

D-Fructose
57-48-7

D-Fructose

A

5-(n-propoxymethyl)-2-furancarboxadehyde
1917-66-4

5-(n-propoxymethyl)-2-furancarboxadehyde

B

Dipropyl ether
111-43-3

Dipropyl ether

C

propyl methanoate
110-74-7

propyl methanoate

D

n-propyl levulinate
645-67-0

n-propyl levulinate

Conditions
ConditionsYield
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%
propan-1-ol
71-23-8

propan-1-ol

dihydroxyacetone
96-26-4

dihydroxyacetone

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With Cu/Al2O3; dihydrogen peroxide In chloroform at 80℃; for 24h;83%
propan-1-ol
71-23-8

propan-1-ol

phenylacetylene
536-74-3

phenylacetylene

A

propyl methanoate
110-74-7

propyl methanoate

B

propyl benzoate
2315-68-6

propyl benzoate

Conditions
ConditionsYield
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)
121393-39-3

5,10,15,20-tetra(2,4,6-trimethylphenyl)porphyrinate rhodium(II)

Dipropyl ether
111-43-3

Dipropyl ether

(5,10,15,20-tetra(2,4,6-trimethylphenyl)porphyrinato)rhodium(III) ethyl
342790-12-9

(5,10,15,20-tetra(2,4,6-trimethylphenyl)porphyrinato)rhodium(III) ethyl

B

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With water; tetraphenylphosphonium bromide; triphenylphosphine; potassium hydroxide at 25℃; Inert atmosphere; Darkness; regioselective reaction;A 62%
B n/a
2-(tert-butylperoxy)tetrahydrofuran
31144-05-5

2-(tert-butylperoxy)tetrahydrofuran

A

4-butanolide
96-48-0

4-butanolide

B

propyl methanoate
110-74-7

propyl methanoate

C

formic acid 3-tert-butoxypropyl ester

formic acid 3-tert-butoxypropyl ester

D

acetone
67-64-1

acetone

E

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
In various solvent(s) at 120℃; for 14h; Mechanism; Product distribution;A 30%
B 11%
C 12%
D 7%
E 61%
propan-1-ol
71-23-8

propan-1-ol

D-glucose
50-99-7

D-glucose

A

formic acid
64-18-6

formic acid

B

propyl methanoate
110-74-7

propyl methanoate

C

1-Propyl acetate
109-60-4

1-Propyl acetate

D

carbon dioxide
124-38-9

carbon dioxide

E

carbon monoxide
201230-82-2

carbon monoxide

F

acetic acid
64-19-7

acetic acid

Conditions
ConditionsYield
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
621-76-1

tripropyl orthoformate

benzoyl chloride
98-88-4

benzoyl chloride

A

1-Chloropropane
540-54-5

1-Chloropropane

B

propyl methanoate
110-74-7

propyl methanoate

C

propyl benzoate
2315-68-6

propyl benzoate

tripropyl orthoformate
621-76-1

tripropyl orthoformate

acetaldehyde
75-07-0

acetaldehyde

A

acetaldehyde dipropyl acetal
105-82-8

acetaldehyde dipropyl acetal

B

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With sulfuric acid
1,3-dioxane
505-22-6

1,3-dioxane

A

propyl methanoate
110-74-7

propyl methanoate

B

carbon dioxide
124-38-9

carbon dioxide

C

acetaldehyde
75-07-0

acetaldehyde

Conditions
ConditionsYield
In water Product distribution; Mechanism; Irradiation; γ irradiation;
1,3-dioxane
505-22-6

1,3-dioxane

A

propan-1-ol
71-23-8

propan-1-ol

B

formaldehyd
50-00-0

formaldehyd

C

1,3-dioxine
290-13-1

1,3-dioxine

D

ethene
74-85-1

ethene

E

propyl methanoate
110-74-7

propyl methanoate

F

allyl alcohol
107-18-6

allyl alcohol

Conditions
ConditionsYield
Mechanism; Product distribution; Quantum yield; Heating; 185 nm vacuum-ultraviolet photolysis;
1,3-dioxane
505-22-6

1,3-dioxane

A

propyl methanoate
110-74-7

propyl methanoate

B

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
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
505-84-0

dipropoxymethane

tris(ethylsulfanyl)methane
6267-24-9

tris(ethylsulfanyl)methane

A

bis(ethylthio)methane
4396-19-4

bis(ethylthio)methane

B

ethyl propyl sulfide
4110-50-3

ethyl propyl sulfide

C

propyl methanoate
110-74-7

propyl methanoate

D

(ethylthio)propoxymethane

(ethylthio)propoxymethane

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In various solvent(s) at 30℃; Product distribution; equilibrium concentrations; various temperature and reactant ratios, other catalysts;
dipropoxymethane
505-84-0

dipropoxymethane

A

propan-1-ol
71-23-8

propan-1-ol

B

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With ozone In tetrachloromethane at 25℃; Rate constant; k= 0.7 liter/mole.sec;
With ozone In tetrachloromethane at 18℃; Rate constant; Mechanism;
dipropoxymethane
505-84-0

dipropoxymethane

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With di-tert-butyl peroxide at 130℃; Rate constant; kinetic isotope effect; further temperatures;
tripropyl orthoformate
621-76-1

tripropyl orthoformate

A

propane
74-98-6

propane

B

propyl methanoate
110-74-7

propyl methanoate

C

Dipropyl carbonate
623-96-1

Dipropyl carbonate

D

propionaldehyde
123-38-6

propionaldehyde

Conditions
ConditionsYield
With di-tert-butyl peroxide In chlorobenzene at 140℃; for 4h; Kinetics; Mechanism; Product distribution; various temperatures, rates of formation;
carbon monoxide
201230-82-2

carbon monoxide

A

ethanol
64-17-5

ethanol

B

Methyl formate
107-31-3

Methyl formate

C

propyl methanoate
110-74-7

propyl methanoate

D

ethylene glycol
107-21-1

ethylene glycol

Conditions
ConditionsYield
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
81381-75-1

1,3-Bis(1,3-dioxan-2-yloxy)propane

A

trimethylene carbonate
2453-03-4

trimethylene carbonate

B

propyl methanoate
110-74-7

propyl methanoate

C

2-propoxy-1,3-dioxane
85533-20-6

2-propoxy-1,3-dioxane

D

3-([1,3]Dioxan-2-yloxy)-propionaldehyde
85533-24-0

3-([1,3]Dioxan-2-yloxy)-propionaldehyde

E

propyl 3-(1,3-dioxan-2-yloxy)propyl carbonate
85533-23-9

propyl 3-(1,3-dioxan-2-yloxy)propyl carbonate

Conditions
ConditionsYield
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
85533-20-6

2-propoxy-1,3-dioxane

A

trimethylene carbonate
2453-03-4

trimethylene carbonate

B

propane
74-98-6

propane

C

propyl methanoate
110-74-7

propyl methanoate

D

Dipropyl carbonate
623-96-1

Dipropyl carbonate

E

propionaldehyde
123-38-6

propionaldehyde

Conditions
ConditionsYield
With di-tert-butyl peroxide In chlorobenzene at 130℃; Product distribution; Rate constant; Mechanism;
Formic acid 4-formyloxy-3-methyl-butyl ester

Formic acid 4-formyloxy-3-methyl-butyl ester

A

sec-butyl formate
589-40-2

sec-butyl formate

B

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With di-tert-butyl peroxide at 140℃; for 3h; conversion, concentration of products;
2-propoxyethanol
2807-30-9

2-propoxyethanol

A

2-ethyl-1,3-dioxolane
2568-96-9

2-ethyl-1,3-dioxolane

B

propyl methanoate
110-74-7

propyl methanoate

C

n-propoxyacetaldehyde
67365-39-3

n-propoxyacetaldehyde

Conditions
ConditionsYield
With hydroxide at 23.85℃; under 760 Torr; Rate constant; Product distribution; Mechanism;A 5.4 % Chromat.
B 47 % Chromat.
C 15 % Chromat.
propan-1-ol
71-23-8

propan-1-ol

sodium n-propoxide
6819-41-6

sodium n-propoxide

CO

CO

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
Geschwindigkeit der Umsetzung;
Dipropyl ether
111-43-3

Dipropyl ether

A

propyl propionate
106-36-5

propyl propionate

B

propyl methanoate
110-74-7

propyl methanoate

C

acetaldehyde
75-07-0

acetaldehyde

D

propionaldehyde
123-38-6

propionaldehyde

Conditions
ConditionsYield
With nitric oxide Kinetics; Oxidation; UV-irradiation;
propan-1-ol
71-23-8

propan-1-ol

carbon dioxide
124-38-9

carbon dioxide

A

formic acid
64-18-6

formic acid

B

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With hydrogen; triethylamine; TpRu(PPh3)(CH3CN)H at 100℃; under 38000 Torr; for 16h;
propan-1-ol
71-23-8

propan-1-ol

carbon dioxide
124-38-9

carbon dioxide

carbon monoxide
201230-82-2

carbon monoxide

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With hydrogen; potassium carbonate at 169.84℃; under 22502.3 Torr; for 2h;
propan-1-ol
71-23-8

propan-1-ol

Reaxys ID: 11463886

Reaxys ID: 11463886

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
Conversion of starting material;
tetrahydrofuran
109-99-9

tetrahydrofuran

propyl methanoate
110-74-7

propyl methanoate

Conditions
ConditionsYield
With oxygen; [Ru(CO)2Cp]2 under 375.038 Torr; for 168h;
n-Octylamine
111-86-4

n-Octylamine

propyl methanoate
110-74-7

propyl methanoate

N-octylformamide
6282-06-0

N-octylformamide

Conditions
ConditionsYield
With Cp*2Sm(THF)2 In toluene Ambient temperature; further reagent: SmI2;99%
propyl methanoate
110-74-7

propyl methanoate

dibutylamine
111-92-2

dibutylamine

N,N-dibutylformamide
761-65-9

N,N-dibutylformamide

Conditions
ConditionsYield
With Cp*2Sm(THF)2 In toluene Ambient temperature;99%
propyl methanoate
110-74-7

propyl methanoate

(S)-2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-ethyl ester

(S)-2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-ethyl ester

N-tert-butoxycarbonyl-2-benzyloxycarbonyl-4-ethoxycarbonyl-2,3-dihydro-1H-pyrrole

N-tert-butoxycarbonyl-2-benzyloxycarbonyl-4-ethoxycarbonyl-2,3-dihydro-1H-pyrrole

Conditions
ConditionsYield
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%
o-fluorobromobenzene
1072-85-1

o-fluorobromobenzene

propyl methanoate
110-74-7

propyl methanoate

2-Fluorobenzaldehyde
446-52-6

2-Fluorobenzaldehyde

Conditions
ConditionsYield
With magnesium; lithium chloride In tetrahydrofuran; dichloromethane at 20 - 67℃; for 1.5h; Time;91.1%
propyl methanoate
110-74-7

propyl methanoate

1-(Aminomethyl)isoquinoline dihydrochloride
19382-38-8

1-(Aminomethyl)isoquinoline dihydrochloride

2-formamidomethylisoquinoline
58021-71-9

2-formamidomethylisoquinoline

Conditions
ConditionsYield
With TEA In ethanol for 2h; Heating;89%
propyl methanoate
110-74-7

propyl methanoate

p-trifluoromethylphenyl bromide
402-43-7

p-trifluoromethylphenyl bromide

1-propyl 4-(trifluoromethyl)benzoate
959101-12-3

1-propyl 4-(trifluoromethyl)benzoate

Conditions
ConditionsYield
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
110-74-7

propyl methanoate

2,2-diethoxy-ethanamine
645-36-3

2,2-diethoxy-ethanamine

2,2-diethoxy-1-formylaminoethane
53089-10-4

2,2-diethoxy-1-formylaminoethane

Conditions
ConditionsYield
for 3h; Reflux;86%
propyl methanoate
110-74-7

propyl methanoate

benzamide
55-21-0

benzamide

propyl benzoate
2315-68-6

propyl benzoate

Conditions
ConditionsYield
With hydrogenchloride; iron(III) chloride hexahydrate In hexane; water at 80℃; for 14h;86%
Adipic acid
124-04-9

Adipic acid

propyl methanoate
110-74-7

propyl methanoate

A

Hexanedioic acid monopropyl ester
6939-72-6

Hexanedioic acid monopropyl ester

B

di-n-propyl adipate
106-19-4

di-n-propyl adipate

Conditions
ConditionsYield
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
110-74-7

propyl methanoate

quinolin-2-ylmethanamine bischlorohydrate
18004-62-1

quinolin-2-ylmethanamine bischlorohydrate

N-(2-Quinolylmethyl)formamide
63111-81-9

N-(2-Quinolylmethyl)formamide

Conditions
ConditionsYield
With TEA In ethanol for 2h; Heating;83%
propyl methanoate
110-74-7

propyl methanoate

benzoic acid
65-85-0

benzoic acid

propyl benzoate
2315-68-6

propyl benzoate

Conditions
ConditionsYield
With tert.-butylhydroperoxide; copper(II) bis(trifluoromethanesulfonate) In 1,2-dichloro-ethane at 130℃; for 12h; Sealed tube;82%
propyl methanoate
110-74-7

propyl methanoate

aniline
62-53-3

aniline

Formanilid
103-70-8

Formanilid

Conditions
ConditionsYield
With Cp*2Sm(THF)2 In toluene Ambient temperature;80%
propyl methanoate
110-74-7

propyl methanoate

N-cyanoacetamidine
56563-07-6

N-cyanoacetamidine

5-azacytosine
931-86-2

5-azacytosine

Conditions
ConditionsYield
at 115℃; for 2h;80%
oxalyl dichloride
79-37-8

oxalyl dichloride

propyl methanoate
110-74-7

propyl methanoate

dichloromethyl propyl ether
65611-08-7

dichloromethyl propyl ether

Conditions
ConditionsYield
With N-methyl-N-phenylformamide at 60℃; for 9h;76%
propyl methanoate
110-74-7

propyl methanoate

3-(aminomethyl)isoquinoline dihydrochloride

3-(aminomethyl)isoquinoline dihydrochloride

3-formamidomethylisoquinoline
157405-78-2

3-formamidomethylisoquinoline

Conditions
ConditionsYield
With TEA In ethanol for 2h; Heating;75%
deoxyvasicinone
530-53-0

deoxyvasicinone

propyl methanoate
110-74-7

propyl methanoate

α-hydroxymethylenedeoxyvasicin-4-one
62062-74-2

α-hydroxymethylenedeoxyvasicin-4-one

Conditions
ConditionsYield
Stage #1: deoxyvasicinone; propyl methanoate With sodium at 0 - 20℃;
Stage #2: With water Cooling with ice;
75%
propyl methanoate
110-74-7

propyl methanoate

2-(Aminomethyl)-4-methoxyquinoline dihydrochloride
76278-33-6

2-(Aminomethyl)-4-methoxyquinoline dihydrochloride

<(4-Methoxy-2-quinolyl)methyl>formamide
132833-02-4

<(4-Methoxy-2-quinolyl)methyl>formamide

Conditions
ConditionsYield
With TEA In ethanol for 2h; Heating;74%
propyl methanoate
110-74-7

propyl methanoate

dichloromethyl propyl ether
65611-08-7

dichloromethyl propyl ether

Conditions
ConditionsYield
With oxalyl dichloride; N-methyl-N-phenylformamide at 60℃; for 17h;74%
With oxalyl dichloride; N-methyl-N-phenylformamide
propyl methanoate
110-74-7

propyl methanoate

5-(4'-cyanobiphenyl-4-oxy)pentylamine

5-(4'-cyanobiphenyl-4-oxy)pentylamine

1-formamido-5-(4'-cyanobiphenyl-4-oxy)pentane

1-formamido-5-(4'-cyanobiphenyl-4-oxy)pentane

Conditions
ConditionsYield
for 24h; Inert atmosphere; Reflux;73%
styrene
292638-84-7

styrene

propyl methanoate
110-74-7

propyl methanoate

(E)-propyl cinnamate
74513-58-9

(E)-propyl cinnamate

Conditions
ConditionsYield
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
110-74-7

propyl methanoate

N-(2-[2,2-bis(decyloxymethyl)ethoxy]carbonylethyl)amine

N-(2-[2,2-bis(decyloxymethyl)ethoxy]carbonylethyl)amine

N-formyl-[2-(2,2-bis(decyloxymethyl)ethoxy)carbonylethyl]amine

N-formyl-[2-(2,2-bis(decyloxymethyl)ethoxy)carbonylethyl]amine

Conditions
ConditionsYield
With potassium carbonate for 21h; Inert atmosphere; Reflux;68%
propyl methanoate
110-74-7

propyl methanoate

N-[2-(2,2-bis[2,2-di(decyloxymethyl)ethoxymethyl]ethoxy)carbonylethyl]amine

N-[2-(2,2-bis[2,2-di(decyloxymethyl)ethoxymethyl]ethoxy)carbonylethyl]amine

N-formyl-[2-(2,2-bis(2,2-di(decyloxymethyl)ethoxymethyl)ethoxy)carbonylethyl]amine

N-formyl-[2-(2,2-bis(2,2-di(decyloxymethyl)ethoxymethyl)ethoxy)carbonylethyl]amine

Conditions
ConditionsYield
With potassium carbonate for 41h; Inert atmosphere; Reflux;68%
propyl methanoate
110-74-7

propyl methanoate

propan-1-ol
71-23-8

propan-1-ol

Conditions
ConditionsYield
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h;67%
dimethylacetylene
503-17-3

dimethylacetylene

propyl methanoate
110-74-7

propyl methanoate

(2E,5E)-3,5-dimethylhepta-2,5-dien-4-ol
49587-60-2

(2E,5E)-3,5-dimethylhepta-2,5-dien-4-ol

Conditions
ConditionsYield
With isobutylmagnesium bromide; titanocene dichloride65%

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