7787-82-8 Usage
Uses
Used in Adhesives, Sealants, and Coatings Industry:
1-Chloroethyltrichlorosilane is used as a coupling agent for enhancing the adhesion properties of adhesives, sealants, and coatings. It improves the bonding strength between different materials, ensuring durability and performance.
Used in Synthesis of Organosilicon Compounds:
1-Chloroethyltrichlorosilane serves as a precursor in the synthesis of other organosilicon compounds, such as silane coupling agents and silicone elastomers. Its reactivity allows for the creation of a variety of products with diverse applications in various industries.
Safety Precautions:
Due to its high reactivity, 1-Chloroethyltrichlorosilane must be stored and handled in a well-ventilated area and with suitable personal protective equipment to prevent exposure and potential hazards associated with its decomposition products.
Check Digit Verification of cas no
The CAS Registry Mumber 7787-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7787-82:
(6*7)+(5*7)+(4*8)+(3*7)+(2*8)+(1*2)=148
148 % 10 = 8
So 7787-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H4Cl4Si/c1-2(3)7(4,5)6/h2H,1H3
7787-82-8Relevant academic research and scientific papers
Substituted silyl alkylene amines
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, (2008/06/13)
This invention relates to substituted silyl alkylene amines, to the intermediates and processes useful for their preparation, to their pharmacological use as MAO-B inhibitors and to their end-use application in the treatment of Parkinson's Disease and senile dementia of Alzheimer's type.
Packing for use in resolution
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, (2008/06/13)
The packing for use in resolution proposed for the liquid chromatography for particularly the opti-cal resolution of racemic compounds is prepared by reacting a silica gel carrier with a so-called silane treating agent to introduce a spacer part therein and chemically bonding it with a copper salt of a carboxylic or thiocarboxylic acid selected from the group consisting of optically active D- and L-2--acetizinecaroxylic acid, proline, hydroxyproline and allohydroxyproline. The steric bulkiness, the distance between the silica gel and the optically active group and the degree of hydrophobicity are specified so as to obtain an excellent resolving power.
