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CAS

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100198-09-2

Piscidil A, a rotenoid compound isolated from the Chinese herb Piscidia piscipula, belongs to a class of natural products with diverse biological activities. It is known for its potential as an anticancer agent, inducing apoptosis in various cancer cell lines, and also exhibits insecticidal properties, making it a candidate for natural pesticide development. Its unique chemical structure and promising biological activities render Piscidil A a compound of interest for further research and potential use in therapeutic and agricultural applications.

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  • 100198-09-2 Structure

  • Basic information

    1. Product Name: Piscidil A
    2. Synonyms: Piscidil A;Piscidinol A;(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-Pentamethyl-17-((2S,4R,5S)-4,5,6-trihydroxy-6-methylhepta
    3. CAS NO:100198-09-2
    4. Molecular Formula: C30H50O4
    5. Molecular Weight: 474.73
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100198-09-2.mol

  • Chemical Properties

    1. Melting Point: 195 °C(Solv: methanol (67-56-1))
    2. Boiling Point: 599.4±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.09±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.31±0.20(Predicted)
    10. CAS DataBase Reference: Piscidil A(CAS DataBase Reference)
    11. NIST Chemistry Reference: Piscidil A(100198-09-2)
    12. EPA Substance Registry System: Piscidil A(100198-09-2)

  • 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: 100198-09-2(Hazardous Substances Data)

100198-09-2 Usage

Uses

Used in Pharmaceutical Industry:
Piscidil A is used as an anticancer agent for its ability to induce apoptosis in various cancer cell lines, offering a potential therapeutic approach against cancer.
Used in Agricultural Industry:
Piscidil A is used as a natural pesticide due to its insecticidal properties, providing an alternative to synthetic pesticides for pest control in agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 100198-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,9 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100198-09:
(8*1)+(7*0)+(6*0)+(5*1)+(4*9)+(3*8)+(2*0)+(1*9)=82
82 % 10 = 2
So 100198-09-2 is a valid CAS Registry Number.

100198-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (13α,14β,17α,20S,23R,24S)-23,24,25-Trihydroxylanost-7-en-3-one

1.2 Other means of identification

Product number -
Other names Pyruvicacid phenylhydrazone

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:100198-09-2 SDS

100198-09-2Upstream product

100198-09-2Downstream Products

100198-09-2Relevant articles and documents

Cytotoxic quassinoids and tirucallane-type triterpenes from the woods of Eurycoma longifolia

Itokawa,Kishi,Morita,Takeya

, p. 1053 - 1055 (2007/10/02)

New cytostatic quassinoids, 6α-hydroxyeurycomalactone (1), longilactone (2) and 14,15β-dihydroxyklaineanone (3) were isolated from the woods of Eurycoma longifolia (Simaroubaceae) with three cytotoxic quassinoids, 11-dehydroklaineanone (4), eurycomalactone (5) and 5,6-dehydroeurycomalactone (6), and with seven cytotoxic tirucallane-type triterpenes, niloticin (7), dihydroniloticin (8), piscidinol A (9), bourjotinolone A (10), 3-episapelin A (11), melianone (12) and hispidone (13). All of them showed potent cytotoxic activity against P388 and KB cells.

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