Trimethoxy(3-iodopropyl)silane

Trimethoxy(3-iodopropyl)silane - Names and Identifiers

Name	3-Iodopropyltrimethoxysilane
Synonyms	Iodopropyltrimethoxysilane 3-IODOPROPYLTRIMETHOXYSILANE Trimethoxy(iodopropyl)silane 3-Iodopropyltrimethoxysilane 3-Iopdopropyl trimethoxysilane Trimethoxy(3-iodopropyl)silane 1-(Trimethoxysilyl)-3-iodopropane Silane, (3-iodopropyl)trimethoxy-
CAS	14867-28-8
InChI	InChI=1/C6H15IO3Si/c1-8-11(9-2,10-3)6-4-5-7/h4-6H2,1-3H3

Trimethoxy(3-iodopropyl)silane - Physico-chemical Properties

Molecular Formula	C6H15IO3Si
Molar Mass	290.17
Density	1.482g/mLat 20°C(lit.)
Melting Point	<0°C
Boling Point	79-80°C 2mm
Flash Point	72°C
Vapor Presure	0.515mmHg at 25°C
Specific Gravity	1.475
BRN	969628
Storage Condition	2-8°C(protect from light)
Sensitive	7: reacts slowly with moisture/water
Refractive Index	n20/D 1.473(lit.)
Physical and Chemical Properties

Trimethoxy(3-iodopropyl)silane - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	3
FLUKA BRAND F CODES	8-21
TSCA	No
HS Code	29319090

Trimethoxy(3-iodopropyl)silane - Introduction

Is an organosilicon compound with the chemical formula C9H11IO3Si. The following is a description of its nature, use, preparation and safety information:

Nature:
It is a colorless to pale yellow liquid with a unique odor at room temperature. It is soluble in solvents and not readily soluble in water. It belongs to the family of organosilicon compounds and is highly stable and chemically resistant.

Use:
It is widely used as a reagent and catalyst in organic synthesis reactions. It is usually used to mediate coupling reactions between silane and organic functional groups, such as the introduction, reduction and substitution of silane coupling reagents. In addition, it can also be used as a protecting group and a crosslinking agent in organic synthesis.

Method: The phosphonium is generally prepared by a reaction between phenyltrimethoxysilane and an iodoalkyl compound. The common preparation method is to react phenyltrimethoxysilane with iodinated phenyl or iodinated alkyl, and heat and stir under suitable conditions to obtain phosphonium.

Safety Information:
It is necessary to pay attention to safety during use. It is an organic compound that may be irritating and damaging to the skin, eyes and respiratory system. Appropriate personal protective equipment such as gloves, goggles and protective masks are required for operation. In addition, it is recommended to use it in a well-ventilated place to avoid excessive vapor concentration. If accidental contact or inhalation occurs, rinse immediately with clean water and seek medical help.

Last Update：2024-04-10 22:29:15