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123020-21-3

1H-Indole-3-carboxylic acid, 7-iodo-, 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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  • 123020-21-3 Structure

  • Basic information

    1. Product Name: 1H-Indole-3-carboxylic acid, 7-iodo-, Methyl ester
    2. Synonyms: 1H-Indole-3-carboxylic acid, 7-iodo-, Methyl ester;methyl 7-iodo-1H-indole-3-carboxylate;7-Iodo-1H-indole-3-Carbocylic acid methyl ester
    3. CAS NO:123020-21-3
    4. Molecular Formula: C10H8INO2
    5. Molecular Weight: 301.08049
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123020-21-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Indole-3-carboxylic acid, 7-iodo-, Methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole-3-carboxylic acid, 7-iodo-, Methyl ester(123020-21-3)
    11. EPA Substance Registry System: 1H-Indole-3-carboxylic acid, 7-iodo-, Methyl ester(123020-21-3)

  • 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: 123020-21-3(Hazardous Substances Data)

123020-21-3 Usage

Structure

Methyl ester derivative of 7-iodo-1H-indole-3-carboxylic acid

Type of compound

Organic compound

Contains

Indole ring, carboxylic acid functional group, and an iodine atom at the 7th position

Usage

Organic synthesis for the preparation of pharmaceuticals and agrochemicals

Biological activities

Potential anti-inflammatory and anti-cancer properties

Precautions

Potential hazardous properties, should be handled with proper care and by trained professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 123020-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,2 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123020-21:
(8*1)+(7*2)+(6*3)+(5*0)+(4*2)+(3*0)+(2*2)+(1*1)=53
53 % 10 = 3
So 123020-21-3 is a valid CAS Registry Number.

123020-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 7-iodoindole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 7-Iodo-1H-indole-3-carboxylic acid methyl ester

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:123020-21-3 SDS

123020-21-3Relevant articles and documents

Diazonamide synthesis studies: Use of negishi coupling to fashion diazonamide-related biaryls with defined axial chirality

Feldman, Ken S.,Eastman, Kyle J.,Lessene, Guillaume

, p. 3525 - 3528 (2007/10/03)

(matrix presented) The syntheses of a bis indole and an indole salicylate with the required axial chirality for diazonamide A are reported. Atropselectivity in these biaryl systems is enforced by an sp3 stereogenic center in a lactone tether in

Synthesis of analogs of wasabi phytoalexin (methyl 1-methoxyindole-3-carboxylate)

Yamada, Koji,Kanbayashi, Yukiko,Tomioka, Saori,Somei, Masanori

, p. 1627 - 1634 (2007/10/03)

Syntheses of wasabi phytoalexin analogs, such as 6-bromo-5-iodo, 2-bromo-5-iodo, 6-nitro, 5-chloroacetyl, and 6-chloroacetyl congeners, are reported. An interesting effect of the 1-methoxy group on the regioselectivity of electrophilic substitution reactions on indole nucleus is observed.

Syntheses of wasabi phytoalexin (methyl 1-methoxyindole-3-carboxylate) and its 5-iodo derivative, and their nucleophilic substitution reactions

Somei, Masanori,Tanimoto, Asuka,Orita, Hitomi,Yamada, Fumio,Ohta, Toshiharu

, p. 425 - 432 (2007/10/03)

A simple synthetic method for methyl 1-methoxyindole-3-carboxylate, a phytoalexin isolated from Wasabia japonica, syn. Eutrema wasabi, and its 5-iodo derivative is reported. They underwent nucleophilic substitution reactions selectively at the 2-position.

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