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Diisocyanatodimethylsilane, also known as bis(isocyanato)dimethylsilane, is an organosilicon compound with the chemical formula (CH3)2Si(NCO)2. It is a colorless liquid that is sensitive to moisture and air, and it is commonly used as a coupling agent in the production of composite materials, particularly in the rubber and plastics industries. diisocyanatodimethylsilane enhances the adhesion between inorganic fillers and organic polymers, leading to improved mechanical properties and durability of the final product. Diisocyanatodimethylsilane is also utilized in the synthesis of various silicone-based materials and as a cross-linking agent in the production of polyurethane foams. Due to its reactivity, it is essential to handle diisocyanatodimethylsilane with care, using appropriate safety measures to prevent exposure and potential health risks.

5587-62-2

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5587-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5587-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5587-62:
(6*5)+(5*5)+(4*8)+(3*7)+(2*6)+(1*2)=122
122 % 10 = 2
So 5587-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N2O2Si/c1-9(2,5-3-7)6-4-8/h1-2H3

5587-62-2SDS

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 diisocyanato(dimethyl)silane

1.2 Other means of identification

Product number -
Other names Silane,diisocyanatodimethyl

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:5587-62-2 SDS

5587-62-2Relevant academic research and scientific papers

Trimethylsilyl Pseudohalide Adducts of GaCl3 and B(C6F5)3

Bl?sing, Kevin,Bresien, Jonas,Maurer, Steffen,Schulz, Axel,Villinger, Alexander

supporting information, p. 1913 - 1920 (2021/05/10)

Me3Si?X (X=CN, N3, OCN, and SCN) was treated with the Lewis acids GaCl3 and B(C6F5)3 in toluene yielding the desired adducts Me3Si?X→GaCl3 and Me3Si?X→B(C6F5)3. All synthesized adducts were isolated and completely characterized including single crystal structure elucidations. The different structures, thermodynamics of formation and charge transfer effects are discussed on the basis of experimental and theoretical data.

ULTRAVIOLET SPECTROSCOPIC INVESTIGATION OF ISOCYANATO- AND ISOTHIOCYANATO SILANES CONTAINING PHENYL- AND METHYL GROUPS

Veszpremi, Tamas,Barta, Istvan,Nagy, Jozsef

, p. 243 - 250 (2007/10/02)

The members of the series R(n)Si(NCO)(4-n) and R(n)Si(NCS)(4-n), where R = -CH3 and -C6H5, were prepared, their ultraviolet spectra recorded and the observed bands assigned.The spectra were compared to those of halogeno derivatives.The similarity of halogen- and pseudohalogeno-groups and difference between the effect of methyl- and phenyl-groups were studied.

Chemical process

-

, (2008/06/13)

Optionally substituted silicon isocyanates are prepared by reacting a corresponding silicon halide with an alkali metal cyanate or an alkaline earth metal cyanate in an inert solvent having a dielectric constant below about 10, in the presence of a crown ether as a catalyst.

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