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100668-10-8

2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100668-10-8 Structure

  • Basic information

    1. Product Name: 2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)-
    2. Synonyms: 2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)-
    3. CAS NO:100668-10-8
    4. Molecular Formula: C16H15NO3
    5. Molecular Weight: 269.2952
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100668-10-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)-(100668-10-8)
    11. EPA Substance Registry System: 2-PropenaMide, 3-(3,4-dihydroxyphenyl)-N-(phenylMethyl)-(100668-10-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100668-10-8(Hazardous Substances Data)

100668-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100668-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100668-10:
(8*1)+(7*0)+(6*0)+(5*6)+(4*6)+(3*8)+(2*1)+(1*0)=88
88 % 10 = 8
So 100668-10-8 is a valid CAS Registry Number.

100668-10-8SDS

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 CABzA

1.2 Other means of identification

Product number -
Other names -

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:100668-10-8 SDS

100668-10-8Downstream Products

100668-10-8Relevant articles and documents

Electrochemical oxidation of caffeic and ferulic acid derivatives in aprotic medium

Salas-Reyes, Magali,Herna?ndez, Javier,Domi?nguez, Zaira,Gonza?lez, Felipe J.,Astudillo, Pablo D.,Navarro, Rosa Elena,Marti?nez-Benavidez, Evelin,Vela?zquez-Contreras, Carlos,Cruz-Sa?nchez, Samuel

, p. 693 - 701 (2011)

We studied the electrochemical behaviour as a function of the structure of a series of caffeic and ferulic acids derivatives as well as their corresponding redox moieties catechol and guaiacol by cyclic voltammetry. Results revealed that the medium is key

Host-guest complexation of antioxidative caffeic and ferulic acid amides with a functionalized cyclophane

Virues, Claudia,Dominguez, Zaira,Salas, Magali,Navarro, Rosa Elena,Velazquez, Enrique F.,Cruz, Samuel,Hernandez, Javier,Inoue, Motomichi

, p. 407 - 413 (2012)

Host-guest complexation has been studied by 1H NMR on the benzyl and phenethyl amides of ferulic and caffeic acids as the guests in chloroform and acetonitrile; the counter host is a cyclophane which integrates four phenylene rings, amino and a

Synthesis and structure-activity relationship analysis of caffeic acid amides as selective matrix metalloproteinase inhibitors

Shi, Zhi-Hao,Li, Nian-Guang,Shi, Qian-Ping,Tang, Hao,Tang, Yu-Ping,Li, Wei,Yin, Lian,Yang, Jian-Ping,Duan, Jin-Ao

, p. 1206 - 1211 (2013/03/14)

Four series of acid amides were synthesized, and through measurement using a fluorogenic substrate assay with human recombinant MMP-1, MMP-2 and MMP-9, compound 3f showed considerable inhibitory activities against MMP-2, MMP-9 and the best selectivity over MMP-1. Preliminary structure-activity relationship analysis indicated that caffeic acid amides with electron-donating groups at para-position of amino phenyl group showed better inhibitory activities and selectivity than those with electron-withdrawing groups, and the presence of adjacent dihydroxy in the caffeoyl group was very important for the MMP-2 and MMP-9 inhibitory activities.

CATECHOL-BASED DERIVATIVES FOR TREATING OR PREVENTING DIABETICS

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Page/Page column 4; 6, (2009/06/27)

The present invention provides a catechol-based derivative and a pharmaceutical acceptable salt therefrom and a solvate therefrom. A pharmaceutical composition for preventing or treating diabetics and ischemics, comprising a catechol-based derivative of formula (I) and at least one selected from the group consisting of a pharmaceutical excipient, a diluent and a carrier.

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