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17932-62-6

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17932-62-6 Usage

Functional Group

Propiononitrile attached to a triethoxysilyl moiety

Usage

Commonly used as a coupling agent and adhesion promoter

Industrial Applications

Adhesives, sealants, coatings, and composites

Property

Strong binding and cross-linking properties with various substrates

Benefit

Improves adhesion and durability of materials, particularly in polymeric systems

Surface Modifier

For inorganic fillers and reinforcements

Enhanced Properties

Contributes to better mechanical and thermal properties in composites

Role

Plays a crucial role in enhancing the performance and longevity of industrial products

Check Digit Verification of cas no

The CAS Registry Mumber 17932-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17932-62:
(7*1)+(6*7)+(5*9)+(4*3)+(3*2)+(2*6)+(1*2)=126
126 % 10 = 6
So 17932-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H19NO3Si/c1-5-11-14(12-6-2,13-7-3)9(4)8-10/h9H,5-7H2,1-4H3

17932-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-triethoxysilylpropanenitrile

1.2 Other means of identification

Product number -
Other names NCCHMeSi(OEt)3

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:17932-62-6 SDS

17932-62-6Downstream Products

17932-62-6Relevant articles and documents

Reaction of unsaturated nitriles with hydrosilanes

Belyakova,Pomerantseva,Chekrii,Chernyshev,Storozhenko

experimental part, p. 927 - 929 (2011/01/05)

Reaction of acrylonitrile and 1,4-dicyanobut-1-ene with hydrosilanes in the presence of various catalysts was studied. In the presence of triallylamine, allyl-bis(triethoxypropyl)amine, diallylaminopropyltriethoxysilane, HMPA, NiCl2 + 2MePh2PO, CuCl + 2MePh2PO, [(Me 2N)2CCl]2CuCl4, and [(Me 2N)2CCl]2PtCl6, the addition of trichlorosilane to acrylonitrile proceeded with the yield of 36 to 97%. Triethoxy-and tributoxysilane were added to acrylonitrile in the presence of rhodium dicarbonyl acetylacetonate with the formation of α-isomer in 56-58% yield. Attempted addition of hydrosilanes to 1,4-dicyanobutene failed. Pleiades Publishing, Ltd., 2010.

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