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3-(3-chloro-4-hydroxy-5-methoxyphenyl)prop-2-enoic acid is a complex organic compound with the molecular formula C10H9ClO4. It is characterized by a phenyl ring with a chlorine atom at the 3-position, a hydroxyl group at the 4-position, and a methoxy group at the 5-position. The prop-2-enoic acid moiety indicates the presence of a double bond between the first and second carbon atoms of a three-carbon propenoic acid chain, which is attached to the phenyl ring. 3-(3-chloro-4-hydroxy-5-methoxyphenyl)prop-2-enoic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Its chemical structure and functional groups endow it with unique reactivity and properties, making it a valuable component in the field of organic chemistry.

5438-40-4

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5438-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5438-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5438-40:
(6*5)+(5*4)+(4*3)+(3*8)+(2*4)+(1*0)=94
94 % 10 = 4
So 5438-40-4 is a valid CAS Registry Number.

5438-40-4SDS

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 (Z)-3-(3-chloro-4-hydroxy-5-methoxyphenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 5-chloro-4-hydroxy-2-nitro-3-anisaldehyde

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:5438-40-4 SDS

5438-40-4Downstream Products

5438-40-4Relevant academic research and scientific papers

Synthesis of trans-caffeate analogues and their bioactivities against HIV-1 integrase and cancer cell lines

Xia, Chun-nian,Li, Hai-bo,liu, Feng,Hu, Wei-xiao

supporting information; experimental part, p. 6553 - 6557 (2009/09/06)

Forty caffeate analogues were synthesized via a convenient method starting from vanillin with moderate to good yields. The testing of biological activity of these compounds against HIV-1 integrase indicates that four compounds: bornyl caffeate, bornyl 2-nitrocaffeate, 5-nitrocaffeic acid and 5-nitrocaffeic acid phenethyl ester (5-nitroCAPE) possess a good HIV integrase inhibitory activity, IC50 19.9, 26.8, 25.0 and 13.5 μM, respectively. Twelve caffeate analogues were tested by MTT assay on growth of human hepatocellular carcinoma BEL-7404, human breast MCF-7 adenocarcinoma, human lung A549 adenocarcinoma and human gastric cancer BCG823 cell lines, respectively. And the best result is IC50 5.5 μM for CAPE against BEL-7404.

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