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1,8-Bis(trimethylsilylamino)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33285-90-4

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33285-90-4 Usage

Chemical structure

1,8-Bis(trimethylsilylamino)naphthalene consists of a naphthalene ring with two trimethylsilylamino substituents attached at the 1 and 8 positions.

Functional groups

The compound contains trimethylsilylamino groups, which are known for their reactivity and ability to form strong bonds with transition metal centers.

Application in organic synthesis

It is commonly used as a reagent in organic synthesis, particularly in the field of organometallic chemistry.

Reactivity

The trimethylsilylamino groups enhance the reactivity of the compound, allowing it to form strong bonds with transition metal centers and facilitate various chemical reactions.

Synthesis of metal-organic frameworks

1,8-Bis(trimethylsilylamino)naphthalene has been employed in the synthesis of metal-organic frameworks.

Use as a ligand

It is used as a ligand in catalytic processes, contributing to the formation of complex organic and inorganic compounds.

Unique structure

The compound's unique structure and reactivity make it a valuable tool for the preparation of complex organic and inorganic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 33285-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33285-90:
(7*3)+(6*3)+(5*2)+(4*8)+(3*5)+(2*9)+(1*0)=114
114 % 10 = 4
So 33285-90-4 is a valid CAS Registry Number.

33285-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,8-N-bis(trimethylsilyl)naphthalene-1,8-diamine

1.2 Other means of identification

Product number -
Other names -

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:33285-90-4 SDS

33285-90-4Upstream product

33285-90-4Downstream Products

33285-90-4Relevant academic research and scientific papers

Bismuthanylstibanes

Chitnis, Saurabh S.,Marczenko, Katherine M.

, p. 8015 - 8018 (2020/08/03)

Thermally-robust bismuthanylstibanes are prepared in a one-step, high yield reaction, providing the first examples of neutral Bi-Sb σ-bonds in the solid state. DFT calculations indicate that the bis(silylamino)naphthalene scaffold is well-suited for supporting otherwise labile bonds. The reaction chemistry of the Bi-Sb bond is debuted by showing fission using NH3BH3 and insertion of a sulfur atom, the latter providing the first example of a Bi-S-Sb motif. This journal is

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