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163083-64-5

1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,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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  • 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER

    Cas No: 163083-64-5

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  • 163083-64-5 Structure

  • Basic information

    1. Product Name: 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER
    2. Synonyms: 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER;1H-INDOLE-3-CARBOXYLIC ACID,6-METHYL-1-(PHENYLMWETHYL)-,METHYL ESTER
    3. CAS NO:163083-64-5
    4. Molecular Formula: C18H17NO2
    5. Molecular Weight: 279.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163083-64-5.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, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER(163083-64-5)
    11. EPA Substance Registry System: 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,METHYL ESTER(163083-64-5)

  • 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: 163083-64-5(Hazardous Substances Data)

163083-64-5 Usage

Properties

Methyl ester derivative of indole-3-carboxylic acid
Contains a 6-methyl group
Contains a phenylmethyl group

Specific content

1H-Indole-3-carboxylic acid, 6-methyl-1-(phenylmethyl)-, methyl ester is a chemical compound with potential pharmaceutical applications.
It is found in various plant species.
It has been investigated for its potential as a therapeutic agent for various conditions, including cancer and inflammatory diseases.
Researchers aim to enhance its pharmacological properties and improve its bioavailability and effectiveness as a drug candidate by modifying the structure of the indole-3-carboxylic acid with a methyl ester and a phenylmethyl group.
The compound may also have potential applications in the field of organic synthesis and medicinal chemistry due to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 163083-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,8 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 163083-64:
(8*1)+(7*6)+(6*3)+(5*0)+(4*8)+(3*3)+(2*6)+(1*4)=125
125 % 10 = 5
So 163083-64-5 is a valid CAS Registry Number.

163083-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-benzyl-6-methyl-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-INDOLE-3-CARBOXYLIC ACID, 6-METHYL-1-(PHENYLMETHYL)-,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:163083-64-5 SDS

163083-64-5Downstream Products

163083-64-5Relevant articles and documents

A SYNTHESIS OF 6-METHYLINDOLE DERIVATIVES BY METHYLTHIOMETHYLATION AT 6-POSITION IN INDOLE NUCLEUS

Hirano, Satoshi,Akai, Ritsuko,Shinoda, Yoshihiko,Nakatsuka, Shin-ichi

, p. 255 - 258 (2007/10/02)

6-Methylindole derivatives were synthesized by introduction of methylthiomethyl group onto the 6-position of indole nucleus and subsequent desulfurization.

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