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1,3-Cyclohexanedione, 2-(aminomethylene)-5,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32583-56-5

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32583-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32583-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32583-56:
(7*3)+(6*2)+(5*5)+(4*8)+(3*3)+(2*5)+(1*6)=115
115 % 10 = 5
So 32583-56-5 is a valid CAS Registry Number.

32583-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aminomethylene)-5,5-dimethylcyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-aminoethylene-5,5-dimethylcyclohexane-1,3-dione

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:32583-56-5 SDS

32583-56-5Relevant academic research and scientific papers

Iron-catalyzed aminolysis of β-carbonyl 1,3-dithianes: Synthesis of stereodefined β-enaminones and 3,4-disubstituted pyrazoles

Wang, Yeming,Bi, Xihe,Li, Wei-Qi,Li, Dehua,Zhang, Qian,Liu, Qun,Ondon, Brim Stevy

supporting information; experimental part, p. 1722 - 1725 (2011/05/03)

A novel iron-catalyzed aminolysis of β-carbonyl 1,3-dithianes with various amines including ammonia, primary and secondary amines, as well as hydrazine hydrate has been developed, leading to the synthesis of stereodefined β-enaminones and 3,4-disubstitute

NMR of enaminones: Part 4 - 17O NMR study of 2,2-diacylenamines

Zhuo, Jin-Cong

, p. 432 - 440 (2007/10/03)

Natural abundance 17O NMR spectra of 41 2,2-diacylenamines (enamino diketones and enamino diesters), recorded in acetonitrile solution, are reported. Tertiary enamino diketones show only one 17O signal; primary and secondary derivati

ACETALS OF LACTAMS AND ACID AMIDES. 48. REACTION OF ENAMINO DIKETONES WITH AMIDE ACETALS. SYNTHESIS OF DERIVATIVES OF COUMARIN AND CARBOSTYRIL

Grannik, V. G.,Shanazarov, A. K.,Solov'eva, N. P.,Chistyakov, V. V.,Persianova, I. V.,Sheinker, Yu. N.

, p. 1171 - 1177 (2007/10/02)

It was established that the reaction of derivatives of 2-aminomethylenecyclohexane-1,3-dione with N,N-dimethyl-diethylacetal gives dienediamines, heating of which in aqueous hydrochloric acid leads, depending on the structure, to derivatives of carbostyri

Chelating Enaminoketones, I. Syntheses of Asymmetric Ligands

Trathnigg, Bernd,Golob, Karl,Junek, Hans,Perne, Johann,Popitsch, Alois

, p. 1353 - 1368 (2007/10/02)

Syntheses of chelating enaminoketones for a potential use in enrichment or recovery of metals from their aqueous solutions are described.Tridentate ligands were prepared either from aromatic amines, triethoxymethane and cyclic 1,3-dicarbonyl compounds in

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