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T-butyl Phenyl Carbonate

Shop tert-Butyl phenyl carbonate 97 Thermo Scientific at Fisherscifi tert-Butyl phenyl carbonate 97 Thermo Scientific. Organic Building Blocks Chemicals Fisher Scientific English.


Tert Butyl Phenyl Carbonate Sielc

Tert-Butyl phenyl carbonate was used in determination of octanol-water partition coefficients by microemulsion electrokinetic chromatography.

T-butyl phenyl carbonate. Since this compound can be regarded formally as the acid anhydride derived from a tert-butoxycarbonyl group it is commonly referred to as Boc anhydride. TR-B809300 tert-Butyl Phenyl Carbonate Applications tert-Butyl Phenyl Carbonate is used in the synthesis of carbamate protected polyamines as well as in the preparation of small molecule inhibitors of acetyl-CoA carboxylase 1 and 2 modulating long chain fatty acid biosynthesis. Tert-Butyl phenyl carbonate t-Butyl phenyl carbonate 124303_ALDRICH CID81113 NSC60248 EINECS 229-601-8 ZINC00388151 Molecular Formula.

It is also used in the synthesis of 2-nitroindoles and as a reagent for mono-Boc protection of αω-diamines. It also can be called as Carbonic acid11-dimethylethyl phenyl ester and the IUPAC Name about this chemical is tert-butyl phenyl carbonate. Tert-Butyl phenyl carbonate cas.

These carbamate derivatives do not behave as amines which allows certain. This pyrocarbonate reacts with amines to give N-tert-butoxycarbonyl or so-called Boc derivatives. Copy Sheet of paper on top of another sheet.

All 5 China Suppliers 5 Price Available 1 Contractor 2 Recommended Supplier. C 11 H 14 O 3. Benzene and substituted derivatives Benzenoids Fisher Scientific English.

Shop tert-Butyl phenyl carbonate 98 Thermo Scientific at Fishersciat tert-Butyl phenyl carbonate 98 Thermo Scientific. The tert-Butyl phenyl carbonate with its cas register number is 6627-89-0. The second-order rate constant in micelles is smaller than that in water.

Tert-Butyl Phenyl Carbonate is used in the synthesis of carbamate protected polyamines as well as in the preparation of small molecule inhibitors of acetyl-CoA carboxylase 1 and 2 modulating long chain fatty acid biosynthesis. Monoisotopic mass 194094299 Da. It belongs to the following product categories such as Carbonates Carbonyl Compounds Organic Building Blocks and so on.

Shop tert-Butyl phenyl carbonate 98 ACROS Organics at Fisherscifi tert-Butyl phenyl carbonate 98 ACROS Organics. C 11 H 14 O 3. Organic Building Blocks Chemicals Fisher Scientific English.

Tert-Butyl phenyl carbonate C11H14O3 CID 81113 - structure chemical names physical and chemical properties classification patents literature biological activities safetyhazardstoxicity information supplier lists and more. View information documentation regarding tert-Butyl phenyl carbonate including CAS structure more. Spontaneous hydrolysis of t-butyl phenyl carbonate is inhibited by both cationic and anionic micelles.

Chem 2017 82 3245-3251. Shop tert-Butyl phenyl carbonate 97 Thermo Scientific at Fishersciat tert-Butyl phenyl carbonate 97 Thermo Scientific 25g tert-Butyl phenyl carbonate 97 Thermo Scientific Fisher Scientific. Synth 15 2195 2002.

Conversion of tert-butyl esters to other functional groups. C 11 H 14 O 3. Molecular Formula C 11 H 14 O 3.

It was used as reagent for mono-Boc protection of αω-diamines. Find SAFC-B5015 MSDS related peer-reviewed papers technical documents similar products more at Sigma-Aldrich US. Slightly soluble in water.

24-di-tert-butyl-5- 4-oxo-14-dihydroquinoline-3-carboxamidophenyl methyl carbonate. Alfa Chemistry offers tert-Butyl phenyl carbonate for experimental research use. Average mass 194227 Da.

Di-tert-butyl dicarbonate is a reagent widely used in organic synthesis. It was also used in the synthesis of 2-nitroindoles. Tert-Butyl phenyl carbonate is used in determination of octanol-water partition coefficients by microemulsion electrokinetic chromatography.

Tert-Butyl phenyl carbonate structure. The reaction of tert-butyl esters with SOCl 2 at room temperature provides acid chlorides in very good yields whereas benzyl methyl ethyl and isopropyl esters are essentially unreactive.


Butyl Phenyl Carbonate Structure C11h14o3 Over 100 Million Chemical Compounds Mol Instincts


Tert Butyl Phenyl Carbonate 6627 89 0 1h Nmr


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Tert Butyl Phenyl Carbonate 6627 89 0 1h Nmr


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Tert Butyl Phenyl Carbonate 98 Thermo Scientific Fisher Scientific


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Tert Butyl Phenyl Carbonate Sielc


Tert Butyl Phenyl Carbonate 6627 89 0 13c Nmr


Tert Butyl Phenyl Carbonate 6627 89 0 Tci America


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