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100042-33-9

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100042-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100042-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,4 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100042-33:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*2)+(2*3)+(1*3)=39
39 % 10 = 9
So 100042-33-9 is a valid CAS Registry Number.

100042-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(3,4-dihydroxyphenyl)-N-(4-hydroxyphenyl)acrylamide

1.2 Other means of identification

Product number -
Other names 2.4-Dihydroxy-zimtsaeure-(4-hydroxy-anilid)

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:100042-33-9 SDS

100042-33-9Downstream Products

100042-33-9Relevant articles and documents

Synthesis and evaluation of caffeic acid amides as antioxidants

Rajan, Padinchare,Vedernikova, Irina,Cos, Paul,Vanden Berghe, Dirk,Augustyns, Koen,Haemers, Achiel

, p. 215 - 217 (2001)

A series of amides of caffeic acid has been synthesised and their antioxidant properties evaluated as lipid peroxidation inhibitors. Anilides of caffeic acid were found to be very efficient antioxidants with IC50's of 0.3 μM.

Design, synthesis and biological evaluation of caffeic acid amides as selective MMP-2 and MMP-9 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. 343 - 351 (2012/10/29)

Strategy, Management and Health Policy Preclinical Research A series of caffeic acid amides with extended P1' groups were synthesized and tested for their inhibitory activities on matrix metalloproteinase (MMP)-1, MMP-2, and MMP-9. Compound 3f showed considerable inhibitory activities against MMP-2, MMP-9, and best selectivity over MMP-1. Preliminary structure-activity relationship analysis and docking studies indicated that caffeic acid amides with electron-donating groups at p-position of amino phenyl group showed better inhibitory activities and selectivity than those with electron-withdrawing groups. The findings of this study would provide information for the exploitation and utilization of caffeic acid as MMP inhibitor for metastatic tumor treatment.

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