188541-09-5

Basic information

• Product Name: nitroveratryloxycarbonylamidopropyltriethoxysilane,10% in tetrahydrofuran
• Synonyms: nitroveratryloxycarbonylamidopropyltriethoxysilane,10% in tetrahydrofuran;NITROVERATRYLOXYCARBONYLAMIDOPROPYLTRIETHOXYSILANE
• CAS NO: 188541-09-5
• Molecular Formula: C19H32N2O9Si
• Molecular Weight: 460.553
• Mol File: 188541-09-5.mol
• Article Data: 5

Chemical Properties

• Flash Point: -14°C (7°F)
• Appearance: /
• CAS DataBase Reference: nitroveratryloxycarbonylamidopropyltriethoxysilane,10% in tetrahydrofuran(CAS DataBase Reference)
• NIST Chemistry Reference: nitroveratryloxycarbonylamidopropyltriethoxysilane,10% in tetrahydrofuran(188541-09-5)
• EPA Substance Registry System: nitroveratryloxycarbonylamidopropyltriethoxysilane,10% in tetrahydrofuran(188541-09-5)

Safety Data

• Hazardous Substances Data: 188541-09-5(Hazardous Substances Data)

Upstream product

• 42855-00-5 nitroveratryloxycarbonyl chloride 
• 919-30-2 3-aminopropyltriethoxysilane 
• 998-30-1 Triethoxysilane 
• 1016-58-6 6-nitroveratryl alcohol 
• 24801-88-5 3-(triethoxypropyl) isocyanate 

Relevant articles and documents

Synthesis of photosensitive organic-inorganic polymer hybrids by utilizing caged photoactivatable alkoxysilane

Photosensitive polymer hybrids with poly(acrylic acid) (PAA) could be obtained by using caged (photosensitive protecting group modified) alkoxysilane (NVOC-U-PTEOS). Transparent polymer hybrids were prepared with UV irradiation, while the obtained materia

Base-amplifying silicone resins with photobase-generating side chains and their application to negative-working photoresists

To accomplish high photosensitivity of resist systems including photobase generators, we have proposed the concept of base-proliferation reactions that generate base molecules in a nonlinear manner by the action of a catalytic amount of base; however, exc

Wavelength-selective caged surfaces: How many functional levels are possible?

The possibility of wavelength-selective cleavage of seven photolabile caging groups from different families has been studied. Amine-, thiol-, and carboxylic-terminated organosilanes were caged with o-nitrobenzyl (NVOC, NPPOC), benzoin (BNZ), (coumarin-4-yl)methyl (DEACM), 7-nitroindoline (DNI, BNI), and p-hydroxyphenacyl (pHP) derivatives. Caged surfaces modified with the different chromophores were prepared, and their photosensitivity at selected wavelengths was quantified. Different pairs, trios, and quartets of chromophore combinations with wavelength-selective photoresponse were identified. Our results show, for the first time, the possibility of generating surfaces with up to four different and independently addressable functional levels. In addition, this manuscript presents the first systematic comparison of the photolytic properties of different photolabile groups under different irradiation conditions.(Figure Presented)