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75304-04-0

9H-Pyrido[3,4-b]indole-3-carboxylic acid, 1-ethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75304-04-0 Structure

  • Basic information

    1. Product Name: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 1-ethyl-, methyl ester
    2. Synonyms:
    3. CAS NO:75304-04-0
    4. Molecular Formula: C15H14N2O2
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75304-04-0.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: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 1-ethyl-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 1-ethyl-, methyl ester(75304-04-0)
    11. EPA Substance Registry System: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 1-ethyl-, methyl ester(75304-04-0)

  • 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: 75304-04-0(Hazardous Substances Data)

75304-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75304-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75304-04:
(7*7)+(6*5)+(5*3)+(4*0)+(3*4)+(2*0)+(1*4)=110
110 % 10 = 0
So 75304-04-0 is a valid CAS Registry Number.

75304-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-ethyl-9H-pyrido[3,4-b]indole-3-carboxylate

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:75304-04-0 SDS

75304-04-0Downstream Products

75304-04-0Relevant articles and documents

Selenium Dioxide Oxidations in the Indole Area. Synthesis of β-Carboline Alkaloids

Cain, M.,Campos, O.,Guzman, F.,Cook, J.M.

, p. 907 - 913 (1983)

A number of different piperidoindole systems have been subjected to oxidation with selenium dioxide.The bonding between the indole and piperidine unit has been varied to provide different systems, the oxidation of which has led to formation of either 2-acyl- or 3-acylindoles or fully aromatic β-carbolines, depending on the substrate chosen.The pattern of reactivity observed was in complete agreement with the ene mechanism proposed for selenium dioxide oxidations, and this can be employed to predict the regiochemistry of the oxidation.Use of this technology has resulted in a two-step synthesis of the indole alkaloid canthin-6-one (30a).

SELENIUM DIOXIDE OXIDATIONS IN THE β-CARBOLINE AREA

Campos, Olivia,DiPierro, Mike,Cain, Michael,Mantei, Robert,Gawish, Ali,Cook, James M.

, p. 975 - 984 (2007/10/02)

The reaction of 1-ethyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-β-carboline 11 with selenium dioxide has resulted in the synthesis of the β-carboline alkaloids, 1-acetyl-3-methoxycarbonyl-β-carboline 14 and 1-acetyl-β-carboline 15.Application of this technol

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