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161546-33-4

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161546-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161546-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,4 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161546-33:
(8*1)+(7*6)+(6*1)+(5*5)+(4*4)+(3*6)+(2*3)+(1*3)=124
124 % 10 = 4
So 161546-33-4 is a valid CAS Registry Number.

161546-33-4SDS

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 3,5-methanocyclopenta[b]pyrrol-2(1h)-one,hexahydro-1-methyl

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:161546-33-4 SDS

161546-33-4Downstream Products

161546-33-4Relevant articles and documents

Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions

Davies, Jacob,Svejstrup, Thomas D.,Fernandez Reina, Daniel,Sheikh, Nadeem S.,Leonori, Daniele

supporting information, p. 8092 - 8095 (2016/07/16)

The development of photoredox reactions of aryloxy-amides for the generation of amidyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported. Owing to the ease of single-electron-transfer reduction of the aryloxy-amides, the organic dye eosin Y was used as the photoredox catalyst, which results in fully transition-metal-free processes. These transformations exhibit a broad scope, are tolerant to several important functionalities, and have been used in the late-stage modification of complex and high-value N-containing molecules.

Iminyl, Amidyl, and Carbamyl Radicals from O-Benzoyl Oximes and O-Benzoyl Hydroxamic Acid Derivatives.

Boivin, Jean,Callier-Dublanchet, Anne-Claude,Quiclet-Sire, Beatrice,Schiano, Anne-Marie,Zard, Samir Z.

, p. 6517 - 6528 (2007/10/02)

Oxime benzoates and O-benzoyl hydroxamic acid derivatives react with tributylstannane in the presence of AIBN to give iminyl, amidyl, and carbamyl radicals which can be captured by an internal olefin.

Optical and Neutron Inelastic Scattering Study of 2-Methylnorbornanes

Brunel, Yvon,Coulombeau, Christian,Coulombeau, Christiane,Jobic, Herve

, p. 937 - 943 (2007/10/02)

We have measured the infrared, Raman, and neutron vibrational spectra of the 2-methylnorbornanes with a CH3 or CD3 methyl group in the exo or endo position.A normal coordinate analysis has been carried out.The torsional modes of the methyl group are assigned at 240 and 235 cm-1 for the hydrogenated exo and endo isomers, respectively.The corresponding barrier is 15.2 +/- 0.2 kJ mol-1.The calculated neutron intensities are in good agreement with the experimental data.The frequencies are used for the determination of the thermodynamic contribution to the standard free energy difference.

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