Welcome to LookChem.com Sign In|Join Free

CAS

  • or

735240-64-9

2,6-dimethoxy-4-[(propylamino)methyl]phenol is a phenolic compound characterized by the presence of two methoxy groups and a propylamino methyl group attached to its benzene ring. This chemical structure endows it with a variety of potential applications in research and industry, including pharmaceutical and laboratory settings.

735240-64-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 735240-64-9 Structure

  • Basic information

    1. Product Name: 2,6-dimethoxy-4-[(propylamino)methyl]phenol
    2. Synonyms: 2,6-dimethoxy-4-[(propylamino)methyl]phenol
    3. CAS NO:735240-64-9
    4. Molecular Formula: C12H19NO3
    5. Molecular Weight: 225.28416
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 735240-64-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,6-dimethoxy-4-[(propylamino)methyl]phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-dimethoxy-4-[(propylamino)methyl]phenol(735240-64-9)
    11. EPA Substance Registry System: 2,6-dimethoxy-4-[(propylamino)methyl]phenol(735240-64-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 735240-64-9(Hazardous Substances Data)

735240-64-9 Usage

Uses

Used in Pharmaceutical Research:
2,6-dimethoxy-4-[(propylamino)methyl]phenol is utilized as a compound of interest in pharmaceutical research due to its potential antioxidant and antibacterial properties. Its unique structure allows it to be explored for various therapeutic applications.
Used in Laboratory Settings:
As a laboratory reagent, 2,6-dimethoxy-4-[(propylamino)methyl]phenol is employed for its chemical properties, making it a valuable tool in scientific experiments and analyses.
Used in Parkinson's Disease Treatment:
2,6-dimethoxy-4-[(propylamino)methyl]phenol is being studied for its potential use in the treatment of Parkinson's disease, indicating its possible role as a therapeutic agent in neurodegenerative disorders.
Used as an Analgesic:
2,6-dimethoxy-4-[(propylamino)methyl]phenol is also being investigated for its potential as an analgesic, suggesting that it could be used to alleviate pain in various medical applications.
Used as an Anti-Inflammatory Agent:
2,6-dimethoxy-4-[(propylamino)methyl]phenol's anti-inflammatory potential is another area of interest, with research aiming to understand its effects on reducing inflammation and related symptoms.

Check Digit Verification of cas no

The CAS Registry Mumber 735240-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 735240-64:
(8*7)+(7*3)+(6*5)+(5*2)+(4*4)+(3*0)+(2*6)+(1*4)=149
149 % 10 = 9
So 735240-64-9 is a valid CAS Registry Number.

735240-64-9Downstream Products

735240-64-9Relevant articles and documents

Novel caffeic acid amide antioxidants: Synthesis, radical scavenging activity and performance under storage and frying conditions

Aladedunye, Felix,Catel, Yohann,Przybylski, Roman

, p. 945 - 952 (2012/05/05)

Twelve novel dihydro-caffeic acid amides were synthesised in good yields and fully characterised by 1H NMR, 13C NMR, and MS. Their radical scavenging activities were assessed by DPPH assay. Additionally, their abilities to protect polyunsaturated oils under accelerated storage and frying conditions were evaluated. All the new compounds possessed significantly higher radical scavenging activities than α-tocopherol and butylated hydroxytoluene (BHT). The radical scavenging activity of N-decyl-N-(3,5- dimethoxy-4-hydroxybenzyl)-3-(3,4-dihydroxyphenyl) propanamide was 1.7 and 4 times higher than α-tocopherol and BHT, respectively. At the end of the storage period, the respective amounts of hydroperoxides in canola oil triacylglycerols (CTAG) fortified with α-tocopherol and BHT was 6.1 and 1.4 times higher, respectively, than CTAG containing the amide. The frying test showed that CTAG containing N-decyl-N-benzyl-3-(3,4-dihydroxybenzyl) propanamide was 1.3, 1.4, and 1.6 times more stable compared to oil fortified with dihydro-caffeic acid, α-tocopherol and BHT, respectively, as assessed by the amounts of the total polar compounds. Moreover, these compounds were remarkably thermally stable, making them suitable for frying applications.

Benzylamine Antioxidants: Relationship between Structure, Peroxyl Radical Scavenging, Lipid Peroxidation Inhibition, and Cytoprotection

Yu, Melvin J.,McCowan, Jefferson R.,Phebus, Lee A.,Towner, Richard D.,Ho, Peter P. K.,et al.

, p. 1262 - 1271 (2007/10/02)

Three homologous series of 3,5-dialkoxy-4-hydroxybenzylamines were prepared and tested (1) as peroxyl radical scavengers in homogeneous aqueous solution, (2) as inhibitors of iron-dependent peroxidation of rabbit brain vesicular membrane lipids, and (3) a

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 735240-64-9