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Difuran-2-yl(methyl)silyl is a complex organic compound that consists of a silicon atom bonded to a methyl group and a difuran-2-yl group. The difuran-2-yl group is derived from two furan molecules, which are heterocyclic compounds with a five-membered ring containing four carbon atoms and one oxygen atom. difuran-2-yl(methyl)silyl is characterized by its unique structure, which combines the properties of silicon, carbon, and oxygen atoms. It is primarily used in the field of organic synthesis, particularly in the formation of various organosilicon compounds. Due to its stability and reactivity, difuran-2-yl(methyl)silyl plays a significant role in the development of new materials and pharmaceuticals, as well as in the synthesis of other complex organic molecules.

1911-24-6

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1911-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1911-24-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1911-24:
(6*1)+(5*9)+(4*1)+(3*1)+(2*2)+(1*4)=66
66 % 10 = 6
So 1911-24-6 is a valid CAS Registry Number.

1911-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(furan-2-yl)-methylsilicon

1.2 Other means of identification

Product number -
Other names Di-2-furanylmethylsilane

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:1911-24-6 SDS

1911-24-6Relevant academic research and scientific papers

Regioselective Rh(I)-catalyzed sequential hydrosilylation toward the assembly of silicon-based peptidomimetic analogues

Min, Geanna K.,Skrydstrup, Troels

experimental part, p. 5894 - 5906 (2012/09/21)

A highly regioselective Rh(I)-catalyzed hydrosilylation of enamides is presented. This mild protocol allows access to a wide variety of different arylsilanes with substitution at the β-position of the enamide and functionalization on the alkyl chain tethered to the silane. This protocol is extended to include a sequential one-pot hydrosilylation. Using diphenylsilane as the appendage point, hydrosilylation of a protected allyl alcohol followed by hydrosilylation of an enamide generates a complex organosilane in one step. This highly convergent strategy to synthesize these functionalized systems now provides a way for the rapid assembly of a diverse collection of silane-based peptidomimetic analogues.

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