Amino Acids, Proteins and Nucleic Acids
                        
                    
                
                        
                            
                            
                            
                            Alcohols, Phenols and Ethers
                        
                    
                
                        
                            
                            
                            
                            Organo Silicon Compounds
                        
                    
                
                        
                            
                            
                            
                            Halides
                        
                    
                
                        
                            
                            
                            
                            Heterocyclic Compounds
                        
                    
                
                        
                            
                            
                            
                            Organic Fluorine Compounds
                        
                    
                
                        
                            
                            
                            
                            Nitrogen Compounds
                        
                    
                
                        
                            
                            
                            
                            Organometallic Compounds
                        
                    
                
                        
                            
                            
                            
                            Esters
                        
                    
                
                        
                            
                            
                            
                            Hydrocarbons
                        
                    
                
                        
                            
                            
                            
                            Aromatic Compounds
                        
                    
                
                        
                            
                            
                            
                            Carboxylic Acids and Derivatives
                        
                    
                
                        
                            
                            
                            
                            Nitriles
                        
                    
                
                        
                            
                            
                            
                            Organometalate
                        
                    
                
                        
                            
                            
                            
                            Aldehydes, Ketones and Quinones
                        
                    
                
                        
                            
                            
                            
                            Carbohydrate
                        
                    
                
                            CAS:106-40-1
                        
                    
                    
                        
                            Molecular Formula:C6H6BrN
                        
                    
                Alias
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                                Para Bromo Aniline; Benzenamine, 4-Bromo-; 4-Bromo-Aniline; Aniline,P-Bromo; 4-Bromobenzenamine; 4-Bromo-Phenylamine; P-Bromoaniline; 4-Bromobenzenamide; Benzenamine,4-Bromo; P-Bromophenylamine; 1-Amino-4-Bromobenzene
                            
                        
                    
                    
                
                        Brief Introduction
                    
                    
                    
                        
                            4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom. Commercially available, this compound may be used as a building block, e.g. in the preparation of p-bromobiphenyl via the Gomberg-Bachmann reaction.
                        
                    
                    
                
                            CAS:107-58-4
                        
                    
                    
                        
                            Molecular Formula:C7H13NO
                        
                    
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                                tert-Butylacrylamide; N-(tert-Butyl)Acrylamide; 2-Propenamide, N-(1,1-Dimethylethyl)-; N-tert-Butylprop-2-Enamide; Acrylamide, N-tert-Butyl-; N-t-Butylacrylamide; n-tert-Butyl Acrylamide; N-(1,1-Dimethylethyl)-2-Propenamide; T-Bu Acrylamide; N-t-Butyl Acrylamide; N-tert.-Butylacrylamide; N-t-Butyl-2-Propenamide; N- Tertiary Butylacrylamide; N-tert-Butylacrylamide,98%; N-tert-Butylacrylamide (TBA); N-tert-Butylacrylamide, 97%; 2-Propenamide,1-Dimethylethyl)-; N-TERT-Butyl-2-Propenamide; N-tert Butyl Acrylamide
                            
                        
                    
                    
                
                        Brief Introduction
                    
                    
                    
                        
                            N-tert-butylacrylamide is a monomer used in the production of polymers. It is an intermediate in organic chemical synthesis. It is widely used in printing and dyeing, medicine and other industries. It can be used as a thickener and personal care products. .
                        
                    
                    
                
                            CAS:111324-04-0
                        
                    
                    
                        
                            Molecular Formula:C22H63N13P4
                        
                    
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                                1-Tert-Butyl-4,4,4-Tris(Dimethylamino)-2,2-Bis[Tris(Dimethylamino)-Phosphoranylide-Namino]-2Lambda5,4Lambda5-Catenadi(Phosphazene); Tert-Butyl-P4; Phosphazene Base P(4)-T-Bu Solution; Schwesinger Phosphazene Base; N-[[tert-Butylimino-bis[[tris(Dimethylamino)-Lambda5-Phosphanylidene]Amino]-Lambda5-Phosphanyl]Imino-bis(Dimethylamino)-Lambda5-Phosphanyl]-N-Methylmethanamine; Phosphazene base P4-t-Bu Solution; P4-Phosphazene T-Bu; Phosphazene Base P(4)-T-Bu Solution,1.0 0 M In N-Hexane; P4-T-Bu Phosphazene Base
                            
                        
                    
                    
                
                            CAS:12772-68-8
                        
                    
                    
                        
                            Molecular Formula:C6H16N2O
                        
                    
                
                            CAS:128-53-0
                        
                    
                    
                        
                            Molecular Formula:C6H7NO2
                        
                    
                Alias
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                                1-Ethyl-1H-Pyrrole-2,5-Dione; Ethvlmaleimide; N-Ethyl-Maleimid; 1H-Pyrrole-2,5-Dione, 1-Ethyl-; 1-Ethylmaleimide; N-Ethyl-Maleimide; Ethylmaleimide; N-Ethylmaleinimid; N-Ethylmaleic Imide; N-Ethvlmaleimide; Usafb-121; Nem; 1-Ethyl-1H-Pyrrole-2,5-Dione~Nem; N-Ethylmaleimide Sigmaultra; N-Ethylmaleimide 99+%; N-Ethylmaleimidea.R.
                            
                        
                    
                    
                
                        Brief Introduction
                    
                    
                    
                        
                            1. A covalent modification reagent for protein cysteine residues.
2. Mercaptoalkylation reagents inactivate NADP dependent isocitrate dehydrogenase and many endonucleases.
3. Increase the current from the M-channel in sympathetic neurons and act as the opener of KCNQ2, KCNQ4, and KCNQ5 channels.
                        
                    
                    
                
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