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methyl (2Z)-4-(octylamino)-4-oxobut-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96775-68-7

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96775-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96775-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96775-68:
(7*9)+(6*6)+(5*7)+(4*7)+(3*5)+(2*6)+(1*8)=197
197 % 10 = 7
So 96775-68-7 is a valid CAS Registry Number.

96775-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(octylamino)-4-oxobut-2-enoate

1.2 Other means of identification

Product number -
Other names METHYL (Z)-3-(OCTYLCARBAMOYL)PROP-2-ENOATE

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:96775-68-7 SDS

96775-68-7Downstream Products

96775-68-7Relevant academic research and scientific papers

Suppression of food intake in Triatoma infestans by N-substituted methyl maleamates

Audino,Masuh,De Licastro,Vassena,Picollo,Zerba

, p. 339 - 343 (2007/10/03)

A series of methyl esters of N-substituted (Z)- and (E)-maleamic acids were synthesized and their effect on food intake measured on fifth-instar nymphs of Triatoma infestans. Suppression of food intake was found only for the (Z)isomers. The initial reaction rate of the synthesized compounds with glutathione (GSH) was calculated from the reaction in vitro of the (z)-isomers. No reaction was observed with the (E)-isomers. Good correlation between the suppression of food intake, measured by its ED50 (effective dose that inhibited feeding of 50% of the population) and the initial reaction rate with GSH and the hydrophobic parameter π, was found.

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