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bis(iodomethyl)(dimethyl)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18243-15-7

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18243-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18243-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,4 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18243-15:
(7*1)+(6*8)+(5*2)+(4*4)+(3*3)+(2*1)+(1*5)=97
97 % 10 = 7
So 18243-15-7 is a valid CAS Registry Number.

18243-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(iodomethyl)-dimethylsilane

1.2 Other means of identification

Product number -
Other names bis-iodomethyl-dimethyl-silane

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:18243-15-7 SDS

18243-15-7Relevant academic research and scientific papers

Side-on Coordination in Isostructural Nitrous Oxide and Carbon Dioxide Complexes of Nickel

Puerta Lombardi, Braulio M.,Gendy, Chris,Gelfand, Benjamin S.,Bernard, Guy M.,Wasylishen, Roderick E.,Tuononen, Heikki M.,Roesler, Roland

, p. 7077 - 7081 (2021)

A nickel complex incorporating an N2O ligand with a rare η2-N,N′-coordination mode was isolated and characterized by X-ray crystallography, as well as by IR and solid-state NMR spectroscopy augmented by 15N-labeling experi

Synthesis of silaproline, a new proline surrogate

Vivet, Bertrand,Cavelier, Florine,Martinez, Jean

, p. 807 - 811 (2000)

The asymmetric synthesis of a new proline surrogate, incorporating the dimethylsilyl group at position 4 of proline using Schollkopf's bis-lactim ether method, is described.

Synthesis method of azetidine silicon precursor compound and method for synthesizing six-membered silicon-nitrogen heterocyclic compound by using azetidine silicon precursor compound

-

Paragraph 0107; 0112; 0116-0117, (2021/06/26)

The invention discloses a synthesis method of an azetidine silicon precursor compound and a method for synthesizing a six-membered silicon nitrogen heterocyclic compound by using the azetidine silicon precursor compound, and belongs to the technical field

SILYL-CONTAINING HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

-

Page/Page column 73-74, (2013/03/28)

The present invention relates to novel Silyl-Containing Heterocyclic Compounds of Formula (I): and pharmaceutically acceptable salts thereof, wherein A, B, C, D, E, F and L are as defined herein. The present invention also relates to compositions comprising at least one Silyl-Containing Heterocyclic Compound, and methods of using the Silyl-Containing Heterocyclic Compounds for treating or preventing HCV infection in a patient.

SILYL-CONTAINING HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

-

Page/Page column 69, (2013/03/28)

The present invention relates to novel Silyl-Containing Heterocyclic Compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein A, B, C, D and R2 are as defined herein. The present invention also relates to compositions comprising at least one Silyl-Containing Heterocyclic Compound, and methods of using the Silyl-Containing Heterocyclic Compounds for treating or preventing HCV infection in a patient.

Resolution of protected silaproline for a gram scale preparation

Martin,Vanthuyne,Miramon,Martinez,Cavelier

experimental part, p. 649 - 655 (2012/10/07)

Silaproline is an analogue of proline, which exhibits similar conformational properties. Moreover, the presence of dimethylsilyl group confers to silaproline a higher lipophilicity as well as an improved resistance to biodegradation. This report describes

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