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Chaparrinone, a diterpenoid compound, is naturally found in the herbaceous plant Salvia leucophylla, also known as the chaparral sage. It is responsible for the plant's characteristic fragrance and has been identified for its potential antimicrobial and anti-inflammatory properties. With its unique chemical structure and biological activities, chaparrinone is a promising molecule for the development of novel drugs and therapeutics in the field of pharmacology and natural product research.

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  • Picras-3-ene-2,16-dione,11,20-epoxy-1,11,12-trihydroxy-, (1b,11b,12a)- (9CI)

    Cas No: 22611-34-3

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

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  • 22611-34-3 Structure
  • Basic information

    1. Product Name: chaparrinone
    2. Synonyms: chaparrinone
    3. CAS NO:22611-34-3
    4. Molecular Formula: C20H26O7
    5. Molecular Weight: 378.418
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22611-34-3.mol
  • Chemical Properties

    1. Melting Point: 238-242 °C
    2. Boiling Point: 626.1°Cat760mmHg
    3. Flash Point: 224.9°C
    4. Appearance: /
    5. Density: 1.45g/cm3
    6. Vapor Pressure: 2.67E-18mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 12.03±0.70(Predicted)
    11. CAS DataBase Reference: chaparrinone(CAS DataBase Reference)
    12. NIST Chemistry Reference: chaparrinone(22611-34-3)
    13. EPA Substance Registry System: chaparrinone(22611-34-3)
  • 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: 22611-34-3(Hazardous Substances Data)

22611-34-3 Usage

Uses

Used in Pharmaceutical Industry:
Chaparrinone is used as a potential antimicrobial agent for its ability to combat various microorganisms, which can be beneficial in treating infections and developing new antibiotics.
Used in Herbal Remedies:
Chaparrinone is used as an anti-inflammatory component in herbal remedies, leveraging its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Drug Development:
Chaparrinone is used as a key molecule in the development of novel pharmaceuticals due to its unique chemical structure and biological activities, which may lead to the creation of new therapeutic agents for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 22611-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,1 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22611-34:
(7*2)+(6*2)+(5*6)+(4*1)+(3*1)+(2*3)+(1*4)=73
73 % 10 = 3
So 22611-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O7/c1-8-4-12(21)16(24)18(3)10(8)5-13-19-7-26-20(25,17(18)19)15(23)9(2)11(19)6-14(22)27-13/h4,9-11,13,15-17,23-25H,5-7H2,1-3H3/t9-,10+,11+,13-,15-,16-,17-,18-,19-,20+/m1/s1

22611-34-3Upstream product

22611-34-3Relevant articles and documents

Bitter Principles of Ailanthus altissima Swingle. Conversion of Ailanthone into Shinjulactone C

Ishibashi, Masami,Tsuyuki, Takahiko,Takahashi, Takeyoshi

, p. 2357 - 2360 (1985)

Ailanthone was converted into shinjulactone C with a hexacyclic 1α,12α:5α,13α-dicyclo-9βH-picrasane skeleton.The key reaction consists of an intramolecular ionic cycloaddition between a pentadienyl cation and an olefin.

New antiulcer quassinoids from Eurycoma longifolia

Tada, H,Yasuda, F,Otani, K,Doteuchi, M,Ishihara, Y,Shiro, M

, p. 345 - 349 (2007/10/02)

A bioassay study of Pasak bumi (Eurycoma longifolia) led to the isolation of four quassinoids, pasakbumin-A (1), -B (2), -C (4), and -D (7).Both pasakbumin-A (= eurycomanone) 1 and pasakbumin-B 2 exhibited potent antiulcer activity.This prompted us to test some modified quassinoids to reveal that ailanthone (8), the main quassinoid of Ailanthus altissima, and its α-epoxide (9) have potent activity and less toxicity.Thus, quassinoids which are generally recognised as antitumor compounds were revealed to have antiulcer activity.

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