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Benzenamine, N-[(dimethylphenylsilyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33183-35-6

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33183-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33183-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,8 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33183-35:
(7*3)+(6*3)+(5*1)+(4*8)+(3*3)+(2*3)+(1*5)=96
96 % 10 = 6
So 33183-35-6 is a valid CAS Registry Number.

33183-35-6SDS

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 (Anilinomethyl)-phenyldimethylsilan

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:33183-35-6 SDS

33183-35-6Relevant academic research and scientific papers

Linear Hydroaminoalkylation Products from Alkyl-Substituted Alkenes

Warsitz, Michael,Doye, Sven

supporting information, p. 15121 - 15125 (2020/10/23)

The regioselective conversion of alkyl-substituted alkenes into linear hydroaminoalkylation products represents a strongly desirable synthetic transformation. In particular, such conversions of N-methylamine derivatives are of great scientific interest, because they would give direct access to important amines with unbranched alkyl chains. Herein, we present a new one-pot procedure that includes an initial alkene hydroaminoalkylation with an α-silylated amine substrate and a subsequent protodesilylation reaction that delivers linear hydroaminoalkylation products with high selectivity from simple alkyl-substituted alkenes. For that purpose, new titanium catalysts have been developed, which are able to activate the α-C?H bond of more challenging α-silylated amine substrates. In addition, a direct relationship between the ligand structure of the new catalysts and the obtained regioselectivity is described.

Design, synthesis, and photodegradation of silicon-containing polyureas

Hwu, Jih Ru,King, Ke Yung

, p. 3805 - 3815 (2007/10/03)

Novel N-phenyl aromatic polyureas containing bis[(N,N′- diphenylureylene)methyl]silane units in the skeleton were designed as a new type of photodegradable polymer. These materials were successfully prepared in 88-93% yields by copolymerization of bis(ani

Design and synthesis of new hypocholesterolemic organosilanes with antioxidant properties

Gotteland,Delhon,Junquero,Oms,Halazy

, p. 533 - 538 (2007/10/03)

(Arylamino)methylsilane derivatives 3 have been prepared and identified as potent inhibitors of human LDL oxidation mediated by copper(II). Combination of this property with the structural requirement of squalene epoxidase inhibitors led to the design and synthesis of the (arylamino)methylsilane derivative 4 which was characterised as the first potent, orally active squalene epoxidase inhibitor with antioxidant properties.

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