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5-Cyclohexene-1,2,4-trione,5-methyl-3-[[(1-methylethyl)amino]methylene]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75371-97-0

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75371-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75371-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,7 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75371-97:
(7*7)+(6*5)+(5*3)+(4*7)+(3*1)+(2*9)+(1*7)=150
150 % 10 = 0
So 75371-97-0 is a valid CAS Registry Number.

75371-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(N-isopropylaminomethylene)-5-methyl-5-cyclohexene-1,2,4-trione

1.2 Other means of identification

Product number -
Other names 3-[1-Isopropylamino-meth-(Z)-ylidene]-5-methyl-cyclohex-5-ene-1,2,4-trione

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:75371-97-0 SDS

75371-97-0Downstream Products

75371-97-0Relevant academic research and scientific papers

ANODIC ACETOXYLATION OF 2-HYDROXY-3-METHOXY-5-METHYLBENZALDEHYDE AND ITS SCHIFF BASES

Ohmori, Hidenobu,Matsumoto, Akiteru,Masui, Masaichiro

, p. 1887 - 1891 (2007/10/02)

Anodic oxidation of 2-hydroxy-3-methoxybenzaldehyde (II) in acetonitrile-acetic acid (3:1) containing sodium acetate gave an acetoxylated product in which the acetoxyl group is attached to the side-chain methyl group.On the other hand, oxidation of Schiff bases (I) derived from II under the same conditions gave cyclohexenetriones.The latter products were shown to be formed by further oxidation of the initially formed acetoxylated Schiff bases, in which the acetoxy group is introduced into the ring meta to the hydroxyl group.Keywords - anodic acetoxylation; cyclic voltametry; controlled potential electrolysis; salicylaldehydes; phenolic Schiff bases; cyclohexenetriones

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