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2-Butenedioic acid, 2-(cyclohexylamino)-, dimethyl ester, (Z)- is a chemical compound with the molecular formula C12H19NO4. It is an organic ester derived from 2-butenedioic acid, also known as maleic acid, and features a cyclohexylamine group attached to the 2-position. The compound is characterized by its (Z)-configuration, indicating the geometric arrangement of the double bond in the molecule. This specific arrangement of atoms influences its chemical properties and reactivity. The dimethyl ester form suggests that the carboxylic acid groups of the 2-butenedioic acid have been esterified with methanol, resulting in a less acidic and more stable compound. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

7542-96-3

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7542-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7542-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7542-96:
(6*7)+(5*5)+(4*4)+(3*2)+(2*9)+(1*6)=113
113 % 10 = 3
So 7542-96-3 is a valid CAS Registry Number.

7542-96-3SDS

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 dimethyl 2-(cyclohexylamino)but-2-enedioate

1.2 Other means of identification

Product number -
Other names Cyclohexylamino-fumarsaeure-dimethylester

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:7542-96-3 SDS

7542-96-3Relevant academic research and scientific papers

Oxidation of Enamine-esters with Lead tetra-acetate. Part 1. Products from Some N-Alkylaminofumarates

Carr, Richard M.,Norman, Richard O. C.,Vernon, John M.

, p. 156 - 162 (2007/10/02)

N-Methyl- and N-ethyl-aminofumarates are oxidised by lead tetra-acetate to mixture of heterocyclic polyesters: pyrroles (4), pyridines (6), and pyrrolopyrroles (7).Some other N-alkylaminofumarates afford acyclic oxidative dimers, in which enamine m

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