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Cyclohexanamine, N-[[6'-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)[5,5'-bi-1,3-benzodioxol]-6-yl ]methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61599-77-7

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61599-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61599-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61599-77:
(7*6)+(6*1)+(5*5)+(4*9)+(3*9)+(2*7)+(1*7)=157
157 % 10 = 7
So 61599-77-7 is a valid CAS Registry Number.

61599-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<2''-(5'',5''-dimethyloxazolinyl)>-4,5:4',5'-bis(methylenedioxy)-1,1'-biphenyl-2'-carboxaldehyde cyclohexylimine

1.2 Other means of identification

Product number -
Other names cyclohexyl-[6'-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-[5,5']bi[benzo[1,3]dioxolyl]-6-ylmethylene]-amine

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:61599-77-7 SDS

61599-77-7Downstream Products

61599-77-7Relevant academic research and scientific papers

The Ambient Temperature Ullmann Reaction and Its Application to the Total Synthesis of (+/-)-Steganacin

Ziegler, Frederick E.,Chliwner, Irene,Fowler, Kerry W.,Kanfer, Sheldon J.,Kuo, Stephen J.,Sinha, Nanda D.

, p. 790 - 798 (2007/10/02)

The details of a new method for preparing unsymmetrical biphenyls at room temperature by a modification of the classical Ullmann reaction are discussed.An intramolecularly coordinated organocopper reagent is treated with an aryl iodide bearing a potential coordinating ligand to form the biphenyl.Nitrogen and sulfur have been utilized as ligands and as protecting groups for carbonyls.The application of this methodology to the synthesis of the antileukemic steganacin is detailed.

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