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1,3,5-Trisilapentane, also known as 1,3,5-trisilacyclohexane, is a cyclic compound composed of three silicon atoms and six carbon atoms arranged in a hexagonal ring structure. It is a colorless, volatile liquid with a molecular formula of C6H18Si3. 1,3,5-Trisilapentane is a derivative of cyclohexane, where three of the carbon atoms are replaced by silicon atoms. 1,3,5-Trisilapentane is an organosilicon compound with potential applications in the synthesis of various silicon-containing polymers and materials. Due to its unique structure, it exhibits interesting chemical properties and reactivity, making it a subject of interest in the field of organosilicon chemistry.

5637-99-0

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5637-99-0 Usage

Type of compound

Silane compound

Composition

Three silicon atoms and 18 hydrogen atoms

Physical state at room temperature

Colorless and odorless liquid

Flammability

Highly flammable

Common uses

Precursor in the production of other silicon-containing compounds and materials

Application in semiconductor industry

a. Formation of thin films
b. Source of silicon for chemical vapor deposition processes

Research areas

a. Nanotechnology
b. Building block for novel materials with unique electronic and mechanical properties

Check Digit Verification of cas no

The CAS Registry Mumber 5637-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5637-99:
(6*5)+(5*6)+(4*3)+(3*7)+(2*9)+(1*9)=120
120 % 10 = 0
So 5637-99-0 is a valid CAS Registry Number.

5637-99-0Downstream Products

5637-99-0Relevant academic research and scientific papers

LOW MOLECULAR WEIGHT CARBOSILANES, PRECURSORS THEREOF, AND METHODS OF PREPARATION

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Paragraph 0024, (2013/10/22)

A series of silicon compounds are provided, which are excellent precursors to small carbosilanes, such as 1,3,5-trisilapentane, 2,4,6-trisilaheptane, tris(silylmethyl)silane and tetrakis(silylmethyl)silane. A method of preparing a carbosilane involves forming a Grignard, lithium, or metallic reagent from a halomethyltrialkoxysilane, reacting the Grignard, lithium, or metallic reagent with a dihalodihydridosilane, a trihalohydridosilane, a tetrahalosilane, a dialkoxydihydridosilane, a trialkoxyhydridosilane, or a tetraalkoxysilane to yield a carbosilane precursor, and reducing the precursor to form the carbosilane.

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