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68149-78-0

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68149-78-0 Usage

Description

2-Propenal, 3-(3,4-dihydroxyphenyl)is a chemical compound with the molecular formula C9H8O3. It is an aldehyde that contains a 3-(3,4-dihydroxyphenyl) group. 2-Propenal, 3-(3,4-dihydroxyphenyl)is commonly found in plant-based foods such as fruits, vegetables, and grains. It possesses antioxidant properties due to the presence of phenolic groups in its structure. Additionally, it has been studied for its potential use in pharmaceuticals, as it exhibits antimicrobial and anti-inflammatory properties. Overall, 2-Propenal, 3-(3,4-dihydroxyphenyl)has a range of potential applications in the food, health, and pharmaceutical industries.

Uses

Used in Food Industry:
2-Propenal, 3-(3,4-dihydroxyphenyl)is used as a natural antioxidant in the food industry to extend the shelf life of plant-based foods such as fruits, vegetables, and grains. Its antioxidant properties help to prevent oxidation and spoilage, maintaining the freshness and quality of these foods.
Used in Health Industry:
2-Propenal, 3-(3,4-dihydroxyphenyl)is used as a dietary supplement in the health industry due to its antioxidant properties. It helps to neutralize free radicals in the body, promoting overall health and well-being.
Used in Pharmaceutical Industry:
2-Propenal, 3-(3,4-dihydroxyphenyl)is used as an antimicrobial agent in the pharmaceutical industry to combat various types of bacteria and infections. Its antimicrobial properties make it a promising candidate for the development of new antibiotics.
2-Propenal, 3-(3,4-dihydroxyphenyl)is also used as an anti-inflammatory agent in the pharmaceutical industry to reduce inflammation and alleviate pain. Its anti-inflammatory properties make it a potential candidate for the treatment of various inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 68149-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68149-78:
(7*6)+(6*8)+(5*1)+(4*4)+(3*9)+(2*7)+(1*8)=160
160 % 10 = 0
So 68149-78-0 is a valid CAS Registry Number.

68149-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name caffeoylaldehyde

1.2 Other means of identification

Product number -
Other names caffeyl aldehyde

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:68149-78-0 SDS

68149-78-0Relevant articles and documents

In vivo Structure-Activity Relationship of Dihydromethysticin in Reducing Nicotine-Derived Nitrosamine Ketone (NNK)-Induced Lung DNA Damage against Lung Carcinogenesis in A/J Mice

Hati, Santanu,Hu, Qi,Huo, Zhiguang,Lu, Junxuan,Xing, Chengguo

, (2022/03/08)

Lung cancer is the leading cause of cancer-related deaths and chemoprevention should be developed. We recently identified dihydromethysticin (DHM) as a promising candidate to prevent NNK-induced lung tumorigenesis. To probe its mechanisms and facilitate its future translation, we investigated the structure-activity relationship of DHM on NNK-induced DNA damage in A/J mice. Twenty DHM analogs were designed and synthesized. Their activity in reducing NNK-induced DNA damage in the target lung tissues was evaluated. The unnatural enantiomer of DHM was identified to be more potent than the natural enantiomer. The methylenedioxy functional moiety did not tolerate modifications while the other functional groups (the lactone ring and the ethyl linker) accommodated various modifications. Importantly, analogs of high structural similarity to DHM with distinct efficacy in reducing NNK-induced DNA damage have been identified. They will serve as chemical probes to elucidate the mechanisms of DHM in blocking NNK-induced lung carcinogenesis.

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