Welcome to LookChem.com Sign In|Join Free

CAS

  • or

17869-27-1

Post Buying Request

17869-27-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

17869-27-1 Usage

Safety Profile

Mildly toxic by ingestion. Asevere skin and eye irritant. When heated todecomposition it emits smoke and acrid fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 17869-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17869-27:
(7*1)+(6*7)+(5*8)+(4*6)+(3*9)+(2*2)+(1*7)=151
151 % 10 = 1
So 17869-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H20N2O3Si/c10-2-1-9-15-12-6-3-11(4-7-13-15)5-8-14-15/h1-10H2

17869-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecan-5-yl)propan-1-amine

1.2 Other means of identification

Product number -
Other names 1-aminopropyl silatrane

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:17869-27-1 SDS

17869-27-1Relevant articles and documents

A Precious-Metal-Free Hybrid Electrolyzer for Alcohol Oxidation Coupled to CO2-to-Syngas Conversion

Abdiaziz, Kaltum,Bajada, Mark A.,Reisner, Erwin,Roessler, Maxie M.,Roy, Souvik,Wagner, Andreas,Warnan, Julien

, p. 15633 - 15641 (2020)

Electrolyzers combining CO2 reduction (CO2R) with organic substrate oxidation can produce fuel and chemical feedstocks with a relatively low energy requirement when compared to systems that source electrons from water oxidation. Here, we report an anodic hybrid assembly based on a (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) electrocatalyst modified with a silatrane-anchor (STEMPO), which is covalently immobilized on a mesoporous indium tin oxide (mesoITO) scaffold for efficient alcohol oxidation (AlcOx). This molecular anode was subsequently combined with a cathode consisting of a polymeric cobalt phthalocyanine on carbon nanotubes to construct a hybrid, precious-metal-free coupled AlcOx–CO2R electrolyzer. After three-hour electrolysis, glycerol is selectively oxidized to glyceraldehyde with a turnover number (TON) of ≈1000 and Faradaic efficiency (FE) of 83 %. The cathode generated a stoichiometric amount of syngas with a CO:H2 ratio of 1.25±0.25 and an overall cobalt-based TON of 894 with a FE of 82 %. This prototype device inspires the design and implementation of nonconventional strategies for coupling CO2R to less energy demanding, and value-added, oxidative chemistry.

Synthesis and reactivity of novel 3-isothiocyanatopropylsilatrane derived from aminopropylsilatrane: X-ray crystal structure and theoretical studies

Singh, Raghubir,Puri, Jugal Kishore,Chahal, Varinder Kaur,Sharma, Raj Pal,Venugopalan, Paloth

, p. 183 - 188 (2010)

A novel silatrane {A figure is presented} containing Si ← N bond (2.160 ?), has been synthesized by the reaction of 3-aminopropylsilatrane (1), dicyclohexylcarbodiimide (2) and CS2. The structure was established by elemental analysis, spectroscopic methods (IR, 1H NMR, 13C NMR and Mass spectroscopy) and X-ray crystallography. It was correlated with theoretical studies such as semiempirical (AM1, PM3, PM3MM and MNDO), Density Functional Theory (B3LYP) and Hartree-Fock at 3-21+G* and 6-31G*(d) levels. The reactivity of compound 3 was studied with some Lewis acids and bases that showed the formation of corresponding adducts (4-7), which were characterized by elemental analysis, IR and NMR (1H, 13C) spectroscopy.

Synthesis of 1-substituted benzoyl aminopropyl silatranes and their biological activities

Li, Zhonghua,Song, Xiuyan,Su, Huaping,Chen, Jing

, p. 475 - 478 (2005)

Silatranes are organosilicon compounds with outstanding biological activities. Eleven substituted benzoyl aminopropyl silatranes(a-k) have been synthesized by the reaction of aminopropyl silatrane with various substituted benzoyl chlorides. IR, 1HNMR, MS and elemental analysis confirmed their structures. The antibacterial test showed that they were efficient against Fusarium and Rhizataonia.

ETCHANT COMPOSITION, METHOD OF ETCHING INSULATING FILM, METHOD OF MANUFACTURING SEMICONDUCTOR DEVICE, AND SILANE COMPOUND

-

Paragraph 0074-0079, (2019/12/06)

An etchant composition includes a silane compound represented by the following Chemical Formula 1: wherein R1 to R6 are independently hydrogen, halogen, a substituted or unsubstituted C1-C20 hydrocarbyl group, a phenyl group, a C1-C20 alkoxy group, a carboxy group, a carbonyl group, a nitro group, a tri (C1-C20) alkylsilyl group, a phosphoryl group, or a cyano group, L is a direct bond or C1-C3 hydrocarbylene, A is an n-valent radical, and n is an integer of 1 to 4.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17869-27-1