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Nervogenic acid, a natural compound isolated from the fruits of Nervilia fordii, a member of the Orchidaceae family, is recognized for its neuroprotective and anti-inflammatory properties. Nervogenic acid holds promise for therapeutic intervention in neurodegenerative diseases, potentially offering a novel avenue for the treatment of conditions such as Alzheimer's and Parkinson's disease. Its capacity to mitigate inflammation and oxidative stress further underscores its potential in medical applications, with preclinical studies indicating its efficacy. However, continued research is essential to elucidate its full spectrum of effects and uses in medicine.

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  • 17622-86-5 Structure
  • Basic information

    1. Product Name: Nervogenic acid
    2. Synonyms: Nervogenic acid;4-Hydroxy-3,5-bis(3-methyl-2-buten-1-yl)benzoic acid
    3. CAS NO:17622-86-5
    4. Molecular Formula: C17H22O3
    5. Molecular Weight: 365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17622-86-5.mol
  • Chemical Properties

    1. Melting Point: 96-97 °C
    2. Boiling Point: 430.6°C at 760 mmHg
    3. Flash Point: 228.3°C
    4. Appearance: /
    5. Density: 1.089g/cm3
    6. Vapor Pressure: 3.53E-08mmHg at 25°C
    7. Refractive Index: 1.562
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 4.71±0.10(Predicted)
    11. CAS DataBase Reference: Nervogenic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: Nervogenic acid(17622-86-5)
    13. EPA Substance Registry System: Nervogenic acid(17622-86-5)
  • 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: 17622-86-5(Hazardous Substances Data)

17622-86-5 Usage

Uses

Used in Pharmaceutical Industry:
Nervogenic acid is used as a neuroprotective agent for its potential therapeutic effects on neurodegenerative diseases such as Alzheimer's and Parkinson's disease. Nervogenic acid's ability to protect neurons and reduce inflammation and oxidative stress positions it as a promising candidate for further development and clinical application in the treatment of these conditions.
Used in Research and Development:
In the field of medical research, nervogenic acid is utilized as a subject of study for its potential applications in reducing inflammation and oxidative stress in the body. Its properties are being investigated to understand better how it may contribute to the prevention or mitigation of various diseases and conditions associated with these factors.
While the provided materials do not specify different industries for the use of nervogenic acid, the primary focus is on its potential pharmaceutical applications and research implications. Further exploration into its properties and mechanisms of action could lead to additional applications in various industries, such as nutraceuticals or cosmetics, where neuroprotective and anti-inflammatory agents are increasingly sought after.

Check Digit Verification of cas no

The CAS Registry Mumber 17622-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17622-86:
(7*1)+(6*7)+(5*6)+(4*2)+(3*2)+(2*8)+(1*6)=115
115 % 10 = 5
So 17622-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H22O3/c1-11(2)5-7-13-9-15(17(19)20)10-14(16(13)18)8-6-12(3)4/h5-6,9-10,18H,7-8H2,1-4H3,(H,19,20)

17622-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Nervogenic acid

1.2 Other means of identification

Product number -
Other names -

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:17622-86-5 SDS

17622-86-5Relevant articles and documents

Myrsinoic acid E, an anti-inflammatory compound from Myrsine seguinii

Makabe, Hidefumi,Miyazaki, Shintaro,Kamo, Tsunashi,Hirota, Mitsuru

, p. 2038 - 2041 (2007/10/03)

The methanolic extract of Myrsine seguinii yielded the novel anti-inflammatory compound, myrsinoic acid E (1), whose structure was elucidated to be 3,5-digeranyl-4-hydroxy benzoic acid. We synthesized 1- and its 3,5-diprenyl (2) and 3,5-difarnesyl analogu

Glycosyl Nervogenic Acid Esters of Carbohydrates from Anodendron affine (Anodendron. VI)

Abe, Fumiko,Yamauchi, Tatsuo

, p. 2712 - 2720 (2007/10/02)

Esters of p-O-glucosyl- and p-O-primverosylnervogenic acid with some carbohydrates (including dambonitol, glucose, and sucrose) were isolated from the seeds, unripened fruits, and caules of Anodendron affine DRUCE.The locations of the nervogenic acid moiety on dambonitol and sucrose were determined on the basis of spectral and chemical evidence.Keywords--Anodendron affine; Apocynacea; 3,5-diprenyl-4-hydroxybenzoic acid; nervogenic acid; 1,3-di-O-methyl-myo-inositol; dambonitol; 5-acyldambonitol; 6-acyldambonitol; 6glc-O-(p-O-glucosyl)nervogenoylsucrose; anodendrosin

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