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4-(3',4'-dimethoxyphenyl)but-3-en-1-ol, also known as DMPB, is a versatile chemical compound belonging to the phenolic family. It is a butenol derivative, characterized by a butyl chain with a double bond and a phenyl ring containing two methoxy groups. DMPB has been studied for its potential medicinal properties, such as antioxidant, anti-inflammatory, and anti-cancer activities. Additionally, it has been investigated for its use in the synthesis of other organic compounds and its potential applications in pharmaceuticals and other industries.

69768-97-4

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69768-97-4 Usage

Uses

Used in Pharmaceutical Industry:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol is used as a medicinal compound for its potential antioxidant, anti-inflammatory, and anti-cancer activities. Its therapeutic properties make it a promising candidate for the development of new drugs and treatments.
Used in Organic Synthesis:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol is used as a key intermediate in the synthesis of other organic compounds. Its unique structure and functional groups allow for various chemical reactions, making it a valuable building block in organic chemistry.
Used in Antioxidant Applications:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol is used as an antioxidant agent, protecting cells and tissues from oxidative damage caused by free radicals. Its antioxidant properties can be utilized in the development of health supplements and nutraceuticals.
Used in Anti-inflammatory Applications:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol is used as an anti-inflammatory agent, helping to reduce inflammation and alleviate pain associated with various conditions. Its anti-inflammatory properties can be applied in the formulation of pharmaceuticals and topical treatments.
Used in Anti-cancer Applications:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol is used as an anti-cancer agent, exhibiting potential inhibitory effects on the growth and progression of cancer cells. Its anti-cancer properties can be explored for the development of novel therapeutic agents in oncology.
Used in Other Industries:
4-(3',4'-dimethoxyphenyl)but-3-en-1-ol has potential applications in various other industries, such as cosmetics, food and beverage, and material science, due to its unique chemical properties and potential benefits. Its versatility allows for exploration in diverse fields beyond pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 69768-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,6 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69768-97:
(7*6)+(6*9)+(5*7)+(4*6)+(3*8)+(2*9)+(1*7)=204
204 % 10 = 4
So 69768-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O3/c1-14-11-7-6-10(5-3-4-8-13)9-12(11)15-2/h3,5-7,9,13H,4,8H2,1-2H3/b5-3+

69768-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4-(3,4-dimethoxyphenyl)but-3-en-1-ol

1.2 Other means of identification

Product number -
Other names Dmp-butenol

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:69768-97-4 SDS

69768-97-4Relevant academic research and scientific papers

Syntheses of Some Constituents of Zingiber cassumunar

Tuntiwachwuttikul, Pittaya,Limchawfar, Burin,Reutrakul, Vichai,Pancharoen, Orasa,Kusamran, Kosan,Byrne, Lindsay T.

, p. 913 - 916 (2007/10/02)

Syntheses of the aromatic compounds cis-3-(2',4',5'-trimetoxyphenyl)-4-cyclohex-1-ene (1), cis-3-(3',4'-dimethoxyphenyl-4-cyclohex-1-ene (2), cis-3-(3',4'-dimethoxyphenyl)-4-cyclohex-1-ene (3), (E)-4-(3',4'-dimethoxyphenyl)but-3-en-1-ol (5), and (E)-4-(3',4'-dimethoxyphenyl)but-3-enyl acetate (6) have been carried out.

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