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N,N,1,1,1-Pentaethylsilanamine is an organosilicon compound with the chemical formula C8H23NSi. It is a colorless liquid at room temperature and is soluble in organic solvents. N,N,1,1,1-pentaethylsilanamine is primarily used as a coupling agent in the production of silicone rubber, silicone resins, and other silicone-based materials. It helps to improve the adhesion between the silicone and other materials, such as fillers, pigments, and fibers. N,N,1,1,1-Pentaethylsilanamine is also used as a reagent in the synthesis of various organosilicon compounds and as a silylating agent in organic synthesis. Due to its reactivity and potential hazards, it is important to handle this chemical with proper safety precautions.

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  • 6022-10-2 Structure
  • Basic information

    1. Product Name: N,N,1,1,1-pentaethylsilanamine
    2. Synonyms: N,N,1,1,1-Pentaethylsilanamine; silanamine, N,N,1,1,1-pentaethyl-
    3. CAS NO:6022-10-2
    4. Molecular Formula: C10H25NSi
    5. Molecular Weight: 187.3977
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6022-10-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 187.701°C at 760 mmHg
    3. Flash Point: 67.32°C
    4. Appearance: N/A
    5. Density: 0.792g/cm3
    6. Vapor Pressure: 0.857mmHg at 25°C
    7. Refractive Index: 1.428
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N,1,1,1-pentaethylsilanamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N,1,1,1-pentaethylsilanamine(6022-10-2)
    12. EPA Substance Registry System: N,N,1,1,1-pentaethylsilanamine(6022-10-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6022-10-2(Hazardous Substances Data)

6022-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6022-10-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6022-10:
(6*6)+(5*0)+(4*2)+(3*2)+(2*1)+(1*0)=52
52 % 10 = 2
So 6022-10-2 is a valid CAS Registry Number.

6022-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(diethyl-amino)silane

1.2 Other means of identification

Product number -
Other names pentaethylsilylamine

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:6022-10-2 SDS

6022-10-2Relevant articles and documents

Wet-chemical synthesis of different bismuth telluride nanoparticles using metal organic precursors-single source vs. dual source approach

Bendt, Georg,Weber, Anna,Heimann, Stefan,Assenmacher, Wilfried,Prymak, Oleg,Schulz, Stephan

, p. 14272 - 14280 (2015/08/18)

Thermolysis of the single source precursor (Et2Bi)2Te 1 in DIPB at 80 °C yielded phase-pure Bi4Te3 nanoparticles, while mixtures of Bi4Te3 and elemental Bi were formed at higher temperatures. In contrast, cubic Bi2Te particles were obtained by thermal decomposition of Et2BiTeEt 2 in DIPB. Moreover, a dual source approach (hot injection method) using the reaction of Te(SiEt3)2 and Bi(NMe2)3 was applied for the synthesis of different pure Bi-Te phases including Bi2Te, Bi4Te3 and Bi2Te3, which were characterized by PXRD, REM, TEM and EDX. The influence of reaction temperature, precursor molar ratio and thermolysis conditions on the resulting material phase was verified. Moreover, reactions of alternate bismuth precursors such as Bi(NEt2)3, Bi(NMeEt)3 and BiCl3 with Te(SiEt3)2 were investigated.

Aminosilylation of arynes with aminosilanes: Synthesis of 2-silylaniline derivatives

Yoshida, Hiroto,Minabe, Takashi,Ohshita, Joji,Kunai, Atsutaka

, p. 3454 - 3456 (2007/10/03)

The nitrogen-silicon σ-bond of aminosilanes added across the triple bond of arynes to give varied 2-silylaniline derivatives straightforwardly. The Royal Society of Chemistry 2005.

Direct Electrophilic Silylation of Terminal Alkynes

Andreev, Aleksey A.,Konshin, Valeri V.,Komarov, Nikolai V.,Rubin, Michael,Brouwer, Chad,Gevorgyan, Vladimir

, p. 421 - 424 (2007/10/03)

(Equation presented) A variety of alkynylsilanes were efficiently prepared via direct silylation of terminal alkynes with aminosilanes in the presence of zinc halides. Base- and nucleophile-sensitive functionalities were perfectly tolerated under the abov

REACTION OF THE NITROGEN-CONTAINING HETEROANALOGS OF ACETALS WITH TRIETHYLSILANE

Khlebnikova, T. D.,Mel'nitskii, I. A.,Kiladze, T. K.,Kantor, E. A.,Popov, Yu. N.,Rakhmankulov, D. L.

, p. 1532 - 1537 (2007/10/02)

The reaction of 1,3-oxaazacycloalkanes with triethylsilane in the presence of a nickel catalyst and zinc halides was investigated.The new compounds of the triethylsilyloxy(dialkylamino)alkane type, i.e., products from the chemospecific cleavage of the heterocycle at the C2-O bond, were isolated and characterized.It was established that triethylsilane can cleave the C-N bond in acyclic aminals with the formation of triethyl(dialkylamino)silanes and tertiary amines.

19-Hydroxy-PGI2 compounds

-

, (2008/06/13)

Prostacyclin and prostacyclin-type derivatives having a 19-hydroxy feature are disclosed, including processes for preparing them and the appropriate intermediates. The compounds are useful for pharmacological purposes such as inhibition of blood platelate aggregation.

2-Decarboxy-2-hydroxymethyl-19-hydroxy-PG1 analogs

-

, (2008/06/13)

Prostaglandin derivatives having a 19,20-didehydro, a 19-hydroxy, or a 19-keto feature are disclosed, including processes for preparing them and the appropriate intermediates. A typical 19-hydroxy compound of this invention is 19-hydroxy-19-methyl-PGF2α, methyl ester, represented by the formula STR1

Bicyclic lactones

-

, (2008/06/13)

Process for preparing bicyclic lactone acrylic aldehydes and ketones of the formula STR1 wherein "n" is one or 2, wherein R1, is hydrogen, methyl, or ethyl, and wherein R4 is hydrogen or a blocking group; and those aldehydes, ketones, and intermediates prepared therein. The aldehydes and ketones are useful intermediates in preparing prostaglandins and analogs having pharmacological utility.

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