130985-36-3

Basic information

• Product Name: (benzyloxycarbonyl)methyl di-tert-butyl phosphate
• Synonyms: (benzyloxycarbonyl)methyl di-tert-butyl phosphate
• CAS NO: 130985-36-3
• Molecular Weight: 358.372
• Mol File: 130985-36-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (benzyloxycarbonyl)methyl di-tert-butyl phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: (benzyloxycarbonyl)methyl di-tert-butyl phosphate(130985-36-3)
• EPA Substance Registry System: (benzyloxycarbonyl)methyl di-tert-butyl phosphate(130985-36-3)

Safety Data

• Hazardous Substances Data: 130985-36-3(Hazardous Substances Data)

Upstream product

• 30379-58-9 benzyl glycolate 
• 117924-33-1 di-tert-butyl N,N-diethylphosphoramidite 
• 139116-03-3 Benzyl 2-(Methanesulfonyl)acetate 
• 68695-48-7 di-tert-butyl phosphoric acid tetra-n-butylammonium salt 

Downstream Products

• 130985-41-0 N-α-acetyl>-L-prolyl>-L-phenylalanyl>-N^α-methyl-L-histydyl>-5(S)-amino-4(S)-hydroxy-2(S)-isopropyl-7-methyloctanoyl>-L-isoleucyl>-(1-oxo-2-pyridyl)methylamine 
• 130985-40-9 N-α-acetyl>l-prolyl>-L-phenylalanyl>-N^α-methyl-L-histydyl>-5(S)-amino-4(S)-hydroxy-2(S)-isopropyl-7-methyloctanoyl>-L-isoleucyl>-2-pyridylmethylamine 

Relevant articles and documents

Nanoscale ionic diodes with tunable and switchable rectifying behavior

(Figure Presented) Nanoscale ionic diodes have attracted interest as circuit elements for development of nanofluidic devices for a variety of applications, including biosensing, constructing artificial cells, and engineering biological batteries. This paper presents a bottom-up, self-assembly approach for constructing nanopores with rectified conductance behavior in a membrane using semisynthetic derivatives of the ion-channel-forming peptide gramicidin A. The capability to individually access each half of a dimeric gramicidin channel makes it possible to generate asymmetric channels in a membrane that exhibit diodelike conductance properties. The modular nature of these self-assembled channels affords the possibility of tuning their rectifying conductance properties by simple replacement of one peptide derivative with another in the membrane. Additionally, introduction of an external stimulus (here, an enzyme) to change the functional group attached to one side of the gramicidin pore induces diodelike conductance behavior in previously nonrectified channels, demonstrating the possibility of switching the conductance properties of these nanopores in situ in a controlled manner. Copyright

ANTIMICROBIAL OXAZOLIDINONE PRODRUGS

This invention includes oxazolidinone prodrug compounds of Formula (I) and Formula (II) as defined herein. The prodrugs are convertible by natural biological processes into an active ingredient possessed of antimicrobial properties useful in treating bact