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2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN, also known as DDF, is a furan derivative with the molecular formula C12H16O4. It is a colorless liquid characterized by a sweet, fruity odor and is soluble in organic solvents such as chloroform and ether. DDF is relatively stable under normal conditions, but its reactivity and potential health hazards should be carefully considered during handling and use. This chemical compound is commonly utilized in the synthesis of pharmaceuticals and natural products, and has garnered interest in medicinal chemistry research due to its potential anti-inflammatory and anticancer properties.

59906-91-1

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59906-91-1 Usage

Uses

Used in Pharmaceutical Synthesis:
2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN is used as a key intermediate in the synthesis of various pharmaceuticals and natural products. Its unique chemical structure and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN is used as a subject of study for its potential anti-inflammatory and anticancer properties. Researchers are exploring its therapeutic potential and investigating its mechanisms of action to develop novel treatments for various diseases.
Used in Anticancer Applications:
2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN is used as a potential anticancer agent in the development of new cancer therapies. Its ability to target and inhibit the growth of cancer cells makes it a promising candidate for further research and development.
Used in Anti-inflammatory Applications:
In the area of anti-inflammatory research, 2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN is used to explore its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions. Its anti-inflammatory properties could lead to the development of new treatments for various inflammatory diseases.
Used in Chemical Research and Development:
2,5-DIHYDRO-2,5-DIMETHOXY-2-DIMETHOXYMETHYLFURAN is used as a chemical compound in research and development for its unique properties and potential applications in various industries. Its reactivity and stability make it a valuable tool for studying chemical reactions and developing new chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 59906-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59906-91:
(7*5)+(6*9)+(5*9)+(4*0)+(3*6)+(2*9)+(1*1)=171
171 % 10 = 1
So 59906-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O5/c1-10-7-5-6-9(13-4,14-7)8(11-2)12-3/h5-8H,1-4H3

59906-91-1SDS

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 5-(dimethoxymethyl)-2,5-dimethoxy-2H-furan

1.2 Other means of identification

Product number -
Other names 2,5-dimethoxy-2,5-dihydro-furan-2-carbaldehyde dimethylacetal

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:59906-91-1 SDS

59906-91-1Relevant articles and documents

On the formation of reductic acid from pentoses or hexuronic acids

Ahmad,Andersson,Olsson,Westerlund

, p. 217 - 222 (2007/10/02)

Careful hydrolysis of (±)-cis- or (±)-trans-tetrahydro-2,5-dimethoxy-2-furaldehyde dimethyl acetal proceeded via 5,5-dimethoxy-4-oxopentanal to give (±)-trans-4-hydroxy-5-methoxy-2-cyclopenenone and (±)-trans-4,5-dihydroxy-2-cylopentenone. The latter product did not isomerize to 2,3-dihydroxy-2-cyclopentenone (reductic acid) on prolonged reaction. Careful hydrolysis of (±)-cis- or (±)-trans-tetrahydro-2, 5-dimethoxy-2-furaldehyde dimethyl acetal proceeded via 5, 5-dimethoxy-4-oxopentanal to give (±)-tran-4-hydroxy-5-methoxy-2-cyclopentenone and (±)-trans-4 ,5-dihydroxy-2-cyclopentenone. The latter product did not isomerize to 2,3-dihydroxy-2-cyclopentenone (reductic acid) on prolonged reaction.

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