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AMINOTRIPHENYLSILANE, also known as Triphenylsilylamine, is an organosilicon compound with the chemical formula (C6H5)3SiNH2. It is characterized by its three phenyl groups attached to a silicon atom, which is connected to an amino group. This unique structure endows it with versatile chemical properties and reactivity, making it a valuable compound in various applications.

4215-80-9

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4215-80-9 Usage

Uses

Used in Pharmaceutical Industry:
AMINOTRIPHENYLSILANE is used as a reagent for the production of 2-Amino-3-hydroxy-indoles, which possess potent in vivo antimalarial activity. These compounds are of significant interest in the development of new antimalarial drugs, as they can potentially offer effective treatment options for malaria.
Used in Catalyst Modification:
AMINOTRIPHENYLSILANE is used to modify Mo/HZSM-5 catalysts, which are employed in the methane-to-benzene (MTB) reaction. The modification with AMINOTRIPHENYLSILANE is predicted to have a positive impact on the selectivity of the reaction, leading to improved efficiency and product yield.
Used in Chemical Research:
AMINOTRIPHENYLSILANE may be used in various chemical research studies, such as:
1. Preparation of dimers of the type [Ti(μ-NR)(NMe2)2]2 (R = 1-adamantyl, (t)Bu, SiPh3), where AMINOTRIPHENYLSILANE serves as a key component in the synthesis process.
2. Silylation during the pretreatment of fused silica capillary surface to achieve a homogeneous film, which is crucial for certain analytical techniques.
3. Preparation of triphenylsilylsulfinylamine, via reaction with thionyl chloride, which can be further utilized in various chemical reactions and applications.
4. To investigate the molecular tuning effect of silanation treatment for HZSM-5 crystals, which can provide insights into the modification of catalyst properties.
5. Synthesis of 9-aminopyrido[3′,3′:4,5]pyrrolo[1,2-c]pyrimidine (9-aminosubstituted derivative), which is an important compound in the field of organic chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 4215-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,1 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4215-80:
(6*4)+(5*2)+(4*1)+(3*5)+(2*8)+(1*0)=69
69 % 10 = 9
So 4215-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,19H2

4215-80-9 Well-known Company Product Price

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  • Aldrich

  • (376205)  Triphenylsilylamine  97%

  • 4215-80-9

  • 376205-5G

  • 1,198.08CNY

  • Detail

4215-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [amino(diphenyl)silyl]benzene

1.2 Other means of identification

Product number -
Other names 1,1,1-triphenylsilanamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4215-80-9 SDS

4215-80-9Relevant academic research and scientific papers

Low-coordinate germylene and stannylene heterocycles featuring sterically tunable bis(amido)silyl ligands

Al-Rafia, S. M. Ibrahim,Lummis, Paul A.,Ferguson, Michael J.,McDonald, Robert,Rivard, Eric

experimental part, p. 9709 - 9717 (2011/01/12)

A series of monomeric heterocyclic metallylenes [{iPr 2Si(NR)2}M:] (M = Ge and Sn; R = Dipp = 2,6- iPr2C6H3 or SiPh3) have been prepared. Preliminary atom-transfer chemistry involving the new low-valent germylenes with the chalcogen sources Me3NO and S8 yielded the corresponding dimeric oxo-and sulfido complexes (e.g., [{ iPr2Si(NDipp)2}Ge-(μ-E)]2; E = O and S). Structural analyses of the metallylenes and their oxidized products reveal that incorporation of the umbrella-shaped triarylsilyl groups (SiPh 3) within the NSiN chelate confers additional steric protection about the group 14 centers relative to a Dipp group. The inclusion of sterically modifiable-SiAr3 (Ar = aryl) units as part of a bis(amido) ligand array represents a new approach in this field and holds considerable promise with regard to attaining increasingly higher degrees of steric bulk.

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