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CAS

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100234-59-1

1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol, commonly known as rutaecarpine, is a naturally occurring quinazolinone alkaloid found in the plant Evodia rutaecarpa. It exhibits a diverse range of pharmacological properties, such as anti-inflammatory, anti-tumor, and cardiovascular effects, making it a promising candidate for drug development and combination therapy.

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  • 100234-59-1 Structure

  • Basic information

    1. Product Name: 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol
    2. Synonyms: 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol;Picrasidine I
    3. CAS NO:100234-59-1
    4. Molecular Formula: C14H12N2O2
    5. Molecular Weight: 240.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100234-59-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 528.2 °C at 760 mmHg
    3. Flash Point: 273.3 °C
    4. Appearance: /
    5. Density: 1.352 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol(100234-59-1)
    11. EPA Substance Registry System: 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol(100234-59-1)

  • 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: 100234-59-1(Hazardous Substances Data)

100234-59-1 Usage

Uses

Used in Pharmaceutical Industry:
1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol is used as a potential therapeutic agent for various conditions, including hypertension, atherosclerosis, and cancer. Its anti-inflammatory, anti-tumor, and cardiovascular effects contribute to its potential in treating these conditions.
Used in Drug Metabolism Regulation:
1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol is used as a regulator of drug metabolism, making it a promising candidate for combination therapy and improving the efficacy of other medications.
Used in Natural Medicine:
1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol is used as an antioxidant and hepatoprotective agent in the field of natural medicine, offering potential benefits for liver health and overall well-being.
Overall, 1-Ethenyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol, or rutaecarpine, has demonstrated a wide range of potential applications across various industries, making it an intriguing compound for further research and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 100234-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,3 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100234-59:
(8*1)+(7*0)+(6*0)+(5*2)+(4*3)+(3*4)+(2*5)+(1*9)=61
61 % 10 = 1
So 100234-59-1 is a valid CAS Registry Number.

100234-59-1SDS

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 4-Methoxy-1-vinyl-9H-β-carbolin-8-ol

1.2 Other means of identification

Product number -
Other names Picrasidine I

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:100234-59-1 SDS

100234-59-1Downstream Products

100234-59-1Relevant articles and documents

Synthetic studies on indoles and related compounds. Part 46.1 First total syntheses of 4, 8-dioxygenated β-carboline alkaloids

Suzuki, Hideharu,Unemoto, Minoru,Hagiwara, Mayumi,Ohyama, Takako,Yokoyama, Yuusaku,Murakami, Yasuoki

, p. 1717 - 1723 (2007/10/03)

Total syntheses of naturally occurring 4, 8-dioxygenated β-carboline alkaloids 2a, 2d, 2g, and 2h are described. The synthetic route involves two methodologies that we developed; (i) an improved Fischer indolization for the synthesis of a 7-oxygenated indole using a tosyl group for protection of the phenolic group, (ii) construction of a 4-methoxy-β-carboline skeleton by the C-3-selective cyclization of the C-2-substituent of the indole nucleus. The phenolic O-tosyl group of the β-carboline skeleton was successfully cleaved to the phenol by Na-anthracenide, and this phenol was methylated with TMSCH2N2.

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