Teflaro; Ceftaroline Fosamil; (6R,7R)-7-[[(2Z)-2-Ethoxyimino-2-[5-(Phosphonoamino)-1,2,4-Thiadiazol-3-Yl]Acetyl]Amino]-3-[[4-(1-Methylpyridin-1-Ium-4-Yl)-1,3-Thiazol-2-Yl]Sulfanyl]-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-Ene-2-Carboxylic Acid,Acetate; Ppi 0903; Ceftaroline Fosamil Acetate Anhydrous; Unii-Ez9W6O5S09; Zinforo

(Methoxymethyl)Triphenylphosphonium Chloride

MSDS

CAS:4009-98-7

Molecular Formula:C20H20ClOP

Alias

More Information

Phosphonium, (Methoxymethyl)Triphenyl-, Chloride; [(Methoxy)Methyl]Tri; [(Methoxy)Methyl]Triphenylphosphonium Chloride; Methoxymethyl Triphenylphosphonium Chloride; Methoxymethyl(Triphenyl)Phosphanium,Chloride

Brief Introduction

(methoxymethyl) triphenylphosphate chloride is used to synthesize cefrataxine, an antiviral and antitumor drug. It is also used to synthesize a fragment of taxol.

4-(Trifluoromethyl)Phenol

MSDS

CAS:402-45-9

Molecular Formula:C7H5F3O

Alias

More Information

4-Trifluoromethylphenol; 4-(Trifluoromethyl)Phenol; α,α,α-Trifluoro-P-Cresol; 4-Hydroxybenzotrifluoride; 4-Hydroxy-α,α,α-Trifluorotoluene; Alpha,Alpha,Alpha-Trifluoro-P-Cresol

Brief Introduction

Three fluoromethyl phenol is an important fluorine containing organic medicine and pesticide intermediate. It can be widely used in the synthesis of various new anticancer drugs, anti AIDS drugs, diabetes drugs, anti-inflammatory drugs, and for the development of insecticides and herbicides.

Diphenylmethoxyphosphine

MSDS

CAS:4020-99-9

Molecular Formula:C13H13OP

Alias

More Information

Methyl Diphenylphosphinite; Methoxydiphenylphosphine; Diphenylphosphinous Acid Methyl Ester; Methoxy(Diphenyl)Phosphane

Lithium Bis(Trimethylsilyl)Amide

MSDS

CAS:4039-32-1

Molecular Formula:C6H18LiNSi2

Alias

More Information

Lithium Hexamethyldisilazide; Hexamethyldisilazane Lithium Salt; Lithiumbis(Trimethylsilyl)Amide; Lithium Bis(Trimethylsilyl)Amide Solution; Lithium Bis(Trimethylsilyl)Azanide; Lithium Hexamethyldisilazane; Lithium;Bis(Trimethylsilyl)Azanide; Lithiumbis(Trimethylsilyl)Amine; Bis(Trimethylsilyl)Amido Lithium; Lithium Tris(Trimethylsilyl)Amine; Lithium Bis(Trimethylsilyl) Amide; Lithium Bis-(Trimethylsilyl)Amide; Lithium, (Bis(Trimethylsilyl)Amino)-; Silanamine, 1,1,1-Trimethyl-N-(Trimethylsilyl)-, Lithium Salt; Lithium Bis[Trimethylsilyl]Amide; Lithium Bistrimethylsilylamide; Lithium Bis-Trimethylsilylamide; Silanamine, 1,1,1-Trimethyl-N-(Trimethylsilyl)-, Lithium Salt (1:1)

Brief Introduction

Lithium bis(trimethylsilyl)amide can be used as a non nucleophilic strong base for the reaction of forming enols, the stereospecific clayson rearrangement of enol esters, the conversion of aldehydes to silimines, and the formation of glycidyl esters, β Lactam reaction and selective cleavage reaction of aryl alkyl ether are mainly used in laboratory research and development process and organic synthesis process.

Inquiry (

/ 10

)

Clear All