Under the optimal conditions, the system showed excellent performance to produce (S)1phenyl1,2ethanediol with an optical purity and a yield both over 99% during the reduction of 2hydroxyacetophenoneShop a large selection of Organooxygen compounds products and learn more about 1Phenyl1,2ethanediol, 97%, ACROS Organics 5g;IS Chemical Technology LTD CAS# Manufacturer China IS Chemical Technology LTD is a pharmaceutical R&D services firm, We offering and the chemical name is 1Phenyl1,2ethanediol
Methyl N Hexyl Ketone 1 Phenyl 1 2 Ethanediol Ketal 2
(r)-(-)-1-phenyl-1 2-ethanediol
(r)-(-)-1-phenyl-1 2-ethanediol-Name(R)()1Phenyl1,2ethanediol,CASPropertiesMolecular FomulaC8H10O2,Molar Mass,Density117g/cm 3 ,Melting Point6568℃,Boling Point273Background (S)1phenyl1,2ethanediol is an important chiral intermediate in the synthesis of liquid crystals and chiral biphosphines (S)carbonyl reductase II from Candida parapsilosis catalyzes the conversion of 2hydroxyacetophenone to (S)1phenyl1,2ethanediol with NADPH as a cofactor
Efficient Production Of S 1 Phenyl 1 2 Ethanediol Using Xylan As Co Substrate By A Coupled Multi Enzyme Escherichia Coli System Microbial Cell Factories Full Text
Shop a large selection of Organooxygen compounds products and learn more about 1Phenyl1,2ethanediol, 97%, ACROS Organics 5g;Objective To realize efficient biosynthesis of 2hydroxyacetophenone to (S)1phenyl1,2ethanediol, we designed a coexpression system containing Candida parapsilosis CCTCC M3011 (S)carbonyl reductase Ⅱ (SCRⅡ) and Bacillus sp YX1 glucose dehydrogenase (GDH) in Escherichia coli BL21(D), based on the optimal ratio between the specific activities of the two enzymes13C NMR of (±)1Phenyl1,2ethanediol
Chiral 1,2diols are a versatile group used in the synthesis of pharmaceuticals, agrochemicals, pheromones and other valuable molecules In particular, (S)1phenyl1,2ethanediol (PED) is a precursor for the production of chiral biphosphines and an initiator for stereoselective polymerization Several methods for the preparation of chiral PED and other 1,2diols have been developed byBuy 1Phenyl1,2ethanediol (CAS ), a product for proteomics research, from Santa Cruz Molecular Formula C6H5CH(OH)CH2OH, MW(±)1Phenyl1,2ethanediol Formula C₆H₅CH(OH)CH₂OH MW g/mol Boiling Pt 272°C 274°C (760mmHg) Melting Pt 61 64 °C Storage Temperature Ambient MDL Number MFCD CAS Number EINECS Merck Index 12, Order Now Specification Test Results
1Phenyl1,2ethanediol C8H10O2 CID 7149 structure, chemical names, physical and chemical properties, classification, patents, literature, biological activitiesVisit ChemicalBook To find more 1Phenyl1,3butanedione() information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes You can also browse global suppliers,vendor,prices,Price,manufacturers of 1Phenyl1,3butanedione()1Phenyl1,2ethanediol 1 Product Result Match Criteria Product Name, Property
S 1 Phenylethane 1 2 Diol 98 0 Tci America Fisher Scientific
1 Phenyl 1 2 Ethanediol 93 56 1 13c Nmr
1,2bis(4methoxyphenyl)1phenyl1,2ethanediol 1 Product Result Match Criteria Product Name Linear Formula C 22 H 22 O 4 Molecular Weight PH ;(R)1phenyl1,2ethanediol is an important synthon for the preparation of βadrenergic blocking agents This study identified a (2R,3R)butanediol dehydrogenase (Kg BDH) from Kurthia gibsonii SC0312, which showed high enantioselectivity for production of (R)1phenyl1,2ethanediol by reduction of 2hydroxyacetophenoneAvantor ®, a Fortune 500 company, is a leading global provider of missioncritical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industriesOur portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve
1 2 Diphenyl 1 2 Ethanediol 655 48 1 C14h14o2 Density Melting Point Boiling Point Structural Formula Synthesis
S 1 Phenyl 1 2 Ethanediol 2 Tosylate Supplier Casno 14 1
13C NMR of (±)1Phenyl1,2ethanediolCompound (±)1Phenyl1,2ethanediolwith free spectra 9 NMR, 11 FTIR, 1 Raman, and 17 MS1Phenyl1,2ethanediol diacetate C12H14O4 CID structure, chemical names, physical and chemical properties, classification, patents, literature
Solved 5 Predict The Products Of Each Of The Following Pi Chegg Com
Propose Synthetic Mechanisms For The 3 Reactions Below No R 1 Phenyl 1 2 Ethanediol S 1 Phenyl 1 2 Ethanediol Homeworklib
(±)1Phenyl1,2ethanediol Formula C₆H₅CH(OH)CH₂OH MW g/mol Boiling Pt 272°C 274°C (760mmHg) Melting Pt 61 64 °C Storage Temperature Ambient MDL Number MFCD CAS Number EINECS Merck Index 12, Order Now Specification Test Results(R)(\u2212)1Phenyl1,2ethanediol (R)(\u2212)1Phenyl1,2ethanediol none European Inventory of Existing Commercial Chemical Substances (EINECS) Not Listed EC Inventory Not Listed United States Toxic Substances Control Act (TSCA) Inventory Not Listed China Catalog of Hazardous chemicals 15 Not Listed(R)(−)1Phenyl1,2ethanediol 99% Synonym (−)Styrene glycol, (R)(−)Phenylethylene glycol CAS Number Linear Formula HOCH 2 CH(C 6 H 5)OH Molecular Weight Beilstein/REAXYS Number MDL number MFCD PubChem Substance ID NACRES N2
Efficient Production Of S 1 Phenyl 1 2 Ethanediol Using Xylan As Co Substrate By A Coupled Multi Enzyme Escherichia Coli System Microbial Cell Factories Full Text
1 4 Trifluoromethyl Phenyl 1 2 Ethanediol C9h9f3o2 Chemspider
Shop a large selection of Organooxygen compounds products and learn more about 1Phenyl1,2ethanediol, 97%, ACROS Organics 5g;Production Industrial routes Ethylene glycol is produced from ethylene (ethene), via the intermediate ethylene oxideEthylene oxide reacts with water to produce ethylene glycol according to the chemical equation C 2 H 4 O H 2 O → HO−CH 2 CH 2 −OH This reaction can be catalyzed by either acids or bases, or can occur at neutral pH under elevated temperaturesAbstract Chiral 1phenyl1,2ethanediol (PED) performs vital effect for the preparation of pharmaceuticals, agrochemicals and cosmetics In the study, a newly isolated strain Kurthia gibsoniiSC0312 with the ability to selectively oxidize racemic PED to achieve (S)PED was evaluated in the aqueous reaction system
S 1 Phenyl 1 2 Ethanediol 2 Tosylate 98 Frontier Scientific
1 Phenyl 1 2 Ethanediol 93 56 1 C8h10o2 Density Melting Point Boiling Point Structural Formula Synthesis
