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855875-40-0

2,4-dihydroxyl-6-pentylbenzaldehyde, also known as vanillin pentyl ether, is a natural chemical compound with a molecular formula C14H18O4. It is a derivative of vanillin, which is a widely used flavoring agent in the food industry. 2,4-dihydroxyl-6-pentylbenzaldehyde is characterized by its sweet, creamy, and slightly fruity odor and is found in the seeds of certain plants. It is recognized for its potential antioxidant and antimicrobial properties, in addition to its applications in the flavor and fragrance industry.

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  • 855875-40-0 Structure

  • Basic information

    1. Product Name: 2,4-dihydroxyl-6-pentylbenzaldehyde
    2. Synonyms: 2,4-dihydroxyl-6-pentylbenzaldehyde
    3. CAS NO:855875-40-0
    4. Molecular Formula:
    5. Molecular Weight: 208.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 855875-40-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-dihydroxyl-6-pentylbenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dihydroxyl-6-pentylbenzaldehyde(855875-40-0)
    11. EPA Substance Registry System: 2,4-dihydroxyl-6-pentylbenzaldehyde(855875-40-0)

  • 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: 855875-40-0(Hazardous Substances Data)

855875-40-0 Usage

Uses

Used in Food Industry:
2,4-dihydroxyl-6-pentylbenzaldehyde is used as a flavoring agent for its distinctive sweet, creamy, and slightly fruity aroma, enhancing the taste and smell of various food products.
Used in Personal Care Products:
In the personal care industry, 2,4-dihydroxyl-6-pentylbenzaldehyde serves as a fragrance ingredient, adding a pleasant scent to products such as perfumes, soaps, and lotions.
Used in Antioxidant Applications:
2,4-dihydroxyl-6-pentylbenzaldehyde is utilized as an antioxidant, potentially protecting food products and other materials from oxidative damage, thus extending their shelf life and maintaining quality.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, 2,4-dihydroxyl-6-pentylbenzaldehyde can be employed as a preservative in various products to inhibit the growth of microorganisms, ensuring safety and longevity.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its antioxidant and antimicrobial properties, 2,4-dihydroxyl-6-pentylbenzaldehyde could also be explored for use in the pharmaceutical industry for the development of new drugs or as an additive in existing medications to enhance their efficacy or stability.

Check Digit Verification of cas no

The CAS Registry Mumber 855875-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,8,7 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 855875-40:
(8*8)+(7*5)+(6*5)+(5*8)+(4*7)+(3*5)+(2*4)+(1*0)=220
220 % 10 = 0
So 855875-40-0 is a valid CAS Registry Number.

855875-40-0Relevant articles and documents

METHOD FOR SYNTHESIS OF LOBARIC ACID AND ANALOG THEREOF

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Paragraph 0074; 0112-0115; ; 0147-0150, (2021/08/13)

The present invention can synthesize lobaric acid and four analogues thereof, which are five phenolic lichen metabolites isolated from an extract of the Antarctic lichen Stereocaulon alpinum and selectively inhibit PTP1B, by a simple, economic and efficient chemical synthesis method.

METHODS FOR SYNTHESIS OF CANNABINOID COMPOUNDS

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, (2020/03/02)

The present invention provides simple synthetic routes for the preparation of cannabinoid compounds such as CBD, CBDV, THC, THCV, CBN, HU-308, CBG, CBC, and derivatives thereof, which are stereoselective and provide the desired cannabinoid compound in high yield.

Total Syntheses of Lobaric Acid and Its Derivatives from the Antarctic Lichen Stereocaulon alpinum

Kim, Tai Kyoung,Kim, Joung Eun,Youn, Ui Joung,Han, Se Jong,Kim, Il-Chan,Cho, Cheon-Gyu,Yim, Joung Han

, p. 1460 - 1467 (2018/06/29)

The first total syntheses of the natural products lobaric acid (1) and its derivatives isolated from the Antarctic lichen Stereocaulon alpinum are reported in this study. Lobarin (3), with a pseudodepsidone structure, was synthesized first in 11 steps by utilizing an Ullmann aryl ether coupling reaction, and lobaric acid was synthesized in an additional three steps by a seven-membered lactonization reaction. Various derivatives were also obtained from the prepared lobaric acid, and the synthetic compounds exhibited significant PTP1B inhibitory activities.

Synthesis and antibacterial evaluation of anziaic acid and its analogues as topoisomerase i inhibitors

Lin, Hao,Annamalai, Thirunavukkarasu,Bansod, Priyanka,Tse-Dinh, Yuk-Ching,Sun, Dianqing

, p. 1613 - 1618 (2013/12/04)

Naturally occurring anziaic acid has very recently been reported as a topoisomerase I inhibitor with antibacterial activity. Herein total synthesis of anziaic acid and its structural analogues is described and the preliminary structure-activity relationship (SAR) has been developed based on topoisomerase inhibition and whole cell antibacterial activity.

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