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Cas:762-75-4
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Type:Trading Company
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Cas:762-75-4
Min.Order:1 Gram
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Cas:762-75-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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
Cas:762-75-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
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Cas:762-75-4
Min.Order:1 Kilogram
FOB Price: $10.0
Type:Trading Company
inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:762-75-4
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
inquiryShandong Mopai Biotechnology 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 chemicals. W
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Cas:762-75-4
Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
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Cas:762-75-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.
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
Cas:762-75-4
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Type:Lab/Research institutions
inquiryWe are a trading company aiming at providing high-quality services to customers. Established for many years, with good reputation in the industry Storage:Sealed and preserved Application:Fine chemical intermediates, used as the main raw material for
Supply top quality products with a reasonable price Application:api
TERT-BUTYL FORMATEAppearance:powder Storage:store in cool, dry place Package:as requested Application:762-75-4 Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by sea LCL/FCL for large a
Stable supply of goods and provision of high-quality services Application:As raw materials in the field of medicine and biology
Good Quality Application:Medical or chemical
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
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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
Cas:762-75-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryplease contact us to confirm the required quantity and quote, we will provide you with COA,NMR,HPLC and other relevant information
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Cas:762-75-4
Min.Order:10 Gram
FOB Price: $1.0 / 2.0
Type:Trading Company
inquiryFINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the TERT-BUTYL FORMATE, CAS:762-75-4 with the most competitive price and the best quality
TERT-BUTYL FORMATEAppearance:powder Storage:store in cool, dry place Package:as requested Application:762-75-4 Transportation:by sea or by air
We are a trading company aiming at providing high-quality services to customers. Established for many years, with good reputation in the industry Storage:Sealed and preserved Application:Fine chemical intermediates, used as the main raw material for
TERT-BUTYL FORMATE Application:762-75-4
Conditions | Yield |
---|---|
In dichloromethane at 40℃; for 72h; | 94% |
Conditions | Yield |
---|---|
In dichloromethane for 144h; Ambient temperature; | 92% |
Conditions | Yield |
---|---|
With silica triflate In hexane for 0.05h; Heating; | 90% |
With sulfuric acid; silica gel In hexane for 0.583333h; Heating; | 85% |
With aminopropylated mesoporous SBA-15 silica at 40℃; for 0.5h; Neat (no solvent); chemoselective reaction; | 80% |
Conditions | Yield |
---|---|
89% | |
89% | |
89% |
di-tert-butyl dicarbonate
tert-butyl formate
Conditions | Yield |
---|---|
In dichloromethane | 75.8% |
tertiary butyl chloride
carbon dioxide
A
tert-butyl formate
B
tert-butyl alcohol
Conditions | Yield |
---|---|
With hydrogen; sodium hydrogencarbonate; {W(CO)5Cl}(1-) In tetrahydrofuran at 150℃; under 80 - 85 Torr; for 24h; | A 73.3% B 26.7% |
Conditions | Yield |
---|---|
With [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II); methacrylic acid methyl ester In toluene at 140℃; under 13689.1 Torr; for 8h; Reagent/catalyst; Autoclave; Inert atmosphere; | 71% |
di-tert-butyl dicarbonate
tert-butyl formate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In 1,4-dioxane; water | 62% |
In 1,4-dioxane; water | |
With sodium hydroxide In 1,4-dioxane |
potassium tert-butylate
dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 50.4% B n/a |
dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 50.4% B n/a |
dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
C
carbon dioxide
Conditions | Yield |
---|---|
With potassium tert-butylate; oxygen In dimethyl sulfoxide at 60℃; Mechanism; other N-methyl-9-(dicarboalkoxymethyl)acridanes; chemiluminescent reaction; | A 50.4% B n/a C n/a |
(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester
potassium tert-butylate
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 18% B n/a |
(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 18% B n/a |
tert-butyl methyl ether
A
acetic acid methyl ester
B
tert-butyl formate
C
acetone
D
tert-butyl alcohol
Conditions | Yield |
---|---|
With ozone In water at 20℃; pH=6.6 - 6.8; Kinetics; Oxidation; ultrasonic irradiation; | A 3% B 8% C 12% D 5% |
With dihydrogen peroxide; iron(II) In water at 21.85℃; pH=3; Kinetics; Further Variations:; irradiation time; UV-irradiation; |
potassium tert-butylate
2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 5.3% B n/a |
2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester
A
10-methyl-9, 10-dihydro-9-acridinone
B
tert-butyl formate
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; | A 5.3% B n/a |
Conditions | Yield |
---|---|
With calcium diformate |
Conditions | Yield |
---|---|
at 60℃; under 130 Torr; |
Conditions | Yield |
---|---|
With sulfuric acid | |
With acidic cation exchanger | |
With sulfuric acid; tert-butyl alcohol at -20℃; |
Conditions | Yield |
---|---|
With ethyl vinyl ether |
di-tert-butoxy-methane
chloroform
A
dichloromethane
B
tertiary butyl chloride
C
tert-butyl formate
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 130℃; Rate constant; Mechanism; |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide In chlorobenzene at 130 - 150℃; Rate constant; Mechanism; or without solvent; |
Conditions | Yield |
---|---|
Thermodynamic data; Mechanism; calculated (BEBO and equibonding method) activation energies for hydrogen atom transfer reaction, anodic formylation; |
Ethyl tert-butyl ether
A
formaldehyd
B
acetic acid tert-butyl ester
C
methyl nitrate
D
tert-butyl formate
Conditions | Yield |
---|---|
With nitrate radical In gas at -16.1 - 89.9℃; under 750.06 Torr; Mechanism; Kinetics; |
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide at 70℃; |
tert-butyl formate
(2,6-bis[(di-tert-butylphosphino)methyl]phenyl)rhodium dinitrogen
(2,6-bis{(di-tert-butylphosphino)methyl}phenyl)carbonylrhodium(III)
Conditions | Yield |
---|---|
In benzene-d6 byproducts: t-BuOH; N2, ligand (1.2-1.5 mmol) added to soln. of Rh compd. (1 mmol), stirred at room temp.; NMR; | 99% |
tert-butyl formate
tert-butyl N-[2-[(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)amino]ethyl]-N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]carbamate
tert-butyl N-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)-N-[2-[tert-butoxycarbonyl-[2-(tert-butyl(dimethyl)silyl)oxyethyl]amino]ethyl]carbamate
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 70℃; for 4h; | 99% |
tert-butyl formate
(+/-)-9-benzyl-3,9-diazabicyclo[4.2.1]nonane-3-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran | 96% |
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran Reflux; | 96% |
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran Reflux; | 95% |
tert-butyl formate
5-chloro-2-methyl-benzenamine
tert-butyl (5-chloro-2-methylphenyl)carbamate
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 16h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With titanium tetrachloride; triethylamine In dichloromethane at -20℃; for 1h; Inert atmosphere; | 94% |
tert-butyl formate
1,1,2,2,3,3-hexafluoro-1-[(1,2,2-trifluoroethenyl)oxy]-3-(trifluoromethoxy)-propane
tert-butyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoate
Conditions | Yield |
---|---|
With at 52 - 55℃; for 24h; Product distribution / selectivity; | 93% |
3-aminobutyric acid
tert-butyl formate
3-t-butoxycarbonylaminobutyric acid
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane; water at 20℃; | 89.2% |
tert-butyl formate
titanium(IV)(N(tert-Bu)(3,5-Me2C6H3))3 formate
Conditions | Yield |
---|---|
In pentane at 24℃; for 0.5h; Inert atmosphere; Schlenk technique; | 88% |
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran Reflux; | 86% |
tert-butyl formate
2-oxabicyclo[3.2.1]octan-3-one
4-[1-Hydroxy-meth-(Z)-ylidene]-2-oxa-bicyclo[3.2.1]octan-3-one
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at 23℃; for 1.5h; | 85% |
Conditions | Yield |
---|---|
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h; | 84% |
chloro-trimethyl-silane
tert-butyl formate
diethyl 3-methylbut-2-enylphosphonate
Conditions | Yield |
---|---|
With hydrogenchloride; lithium diisopropyl amide In tetrahydrofuran at -70℃; 2.) 10 min; 3.) pH=2; | 84% |
tert-butyl formate
1,1,2,3,3-pentafluoro-3-(1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy)prop-1-ene
tert-butyl 2,2,3,4,4-pentafluoro-4-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]butanoate
Conditions | Yield |
---|---|
With at 55 - 58℃; for 32h; | 83% |
Conditions | Yield |
---|---|
With bis(acetylacetonate)oxovanadium In benzene at 20℃; for 0.166667h; | 83% |
tert-butyl formate
tris(trimethylsilyl)silyllithium
bis[tris(trimethylsilyl)silyl]methanol
Conditions | Yield |
---|---|
In pentane at -78℃; | 82% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; for 24h; | 82% |
tert-butyl formate
Conditions | Yield |
---|---|
In not given treatment of tantalum compd. with formate deriv.; | 82% |
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran Reflux; | 82% |
iodobenzene
tert-butyl formate
sodium methylate
A
benzoic acid methyl ester
B
benzoic acid tert-butyl ester
C
benzene
Conditions | Yield |
---|---|
bis-triphenylphosphine-palladium(II) chloride In dichloromethane at 40℃; under 750.06 Torr; for 1h; | A 80% B 11% C 4% |
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