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23652-85-9

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23652-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23652-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,5 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23652-85:
(7*2)+(6*3)+(5*6)+(4*5)+(3*2)+(2*8)+(1*5)=109
109 % 10 = 9
So 23652-85-9 is a valid CAS Registry Number.

23652-85-9SDS

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 4-methylaminopent-3-ene-2-one

1.2 Other means of identification

Product number -
Other names (Z)-4-methylaminopent-3-en-2-one

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:23652-85-9 SDS

23652-85-9Relevant articles and documents

A novel oxidative free radical reaction between 2-hydroxy-1,4-naphthoquinone and β-enamino carbonyl compounds

Chuang, Che-Ping,Wu, Yi-Lung

, p. 1717 - 1719 (2001)

The manganese(III) initiated oxidative free radical reaction between 2-hydroxy-1,4-naphthoquinone and β-enamino carbonyl compound 2 is described. Enamine radical 5 can be generated effectively from the oxidation of enamine 2 by manganese(III) acetate. Spi

Vibrational assignment, structure and intramolecular hydrogen bond of 4-methylamino-3-penten-2-one

Raissi, Heidar,Moshfeghi, Effat,Farzad, Farzaneh

, p. 1004 - 1015 (2005)

The molecular structure, intramolecular hydrogen and vibrational frequencies of 4-methylamino-3-penten-2-one were investigated by a series of density functional theoretical (DFT) calculations and ab initio calculation at the post-Hartree-Fock (MP2) level. Fourier transform infrared and Fourier transform Raman spectra of this compound and its deuterated analogue were clearly assigned. The calculated geometrical parameters show a strong intramolecular hydrogen bond with a N...O distance of 2.622-2.670 A. This bond length is about 0.02 A shorter than that in its parent, 4-amino-3- penten-2-one which is in agreement with spectroscopic results. Furthermore, the conformations of methyl groups with respect to the plane of the molecule and with respect to each other were investigated.

CATALYST COMPOSITION FOR POLYMERIZATION OF OLEFINS

-

, (2015/12/27)

A catalyst composition comprising a monoester, the compound represented by formula (I) as an internal electron donor, and optionally an additional internal electron donor selected from a group consisting of diesters and diethers, wherein: R1, R2, R3, R4, R5 and R6 are hydrogen, straight, branched and cyclic alkyl having at most 20 carbon atoms and aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms, R7 is a straight, branched and cyclic alkyl having at most 20 carbon atoms and aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms, and R8 is an aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms. Also described is a process for preparing the polymerization catalyst composition, a polymerization catalyst system comprising the catalyst composition, a co-catalyst and optionally an external electron donor; and use of the catalyst system for polymerization of olefins.

Functionalized fulgides and fluorophore-photoswitch conjugates

Struebe, Frank,Rath, Susann,Mattay, Jochen

experimental part, p. 4645 - 4653 (2011/10/03)

Various fulgides based on benzofuryl and indolyl core units with versatile functionalities were synthesized. Substitution at the phenylic site shows only small effects on the photochromic properties compared to the parent compounds 30 and 31. Fulgide-dye

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