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93704-52-0

1H-Indol-3-amine,5-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93704-52-0 Structure

  • Basic information

    1. Product Name: 1H-Indol-3-amine,5-methyl-(9CI)
    2. Synonyms: 1H-Indol-3-amine,5-methyl-(9CI);5-Methyl-1H-indol-3-ylaMine
    3. CAS NO:93704-52-0
    4. Molecular Formula: C9H10N2
    5. Molecular Weight: 146.1891
    6. EINECS: N/A
    7. Product Categories: AMINEPRIMARY
    8. Mol File: 93704-52-0.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-Indol-3-amine,5-methyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indol-3-amine,5-methyl-(9CI)(93704-52-0)
    11. EPA Substance Registry System: 1H-Indol-3-amine,5-methyl-(9CI)(93704-52-0)

  • 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: 93704-52-0(Hazardous Substances Data)

93704-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93704-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,0 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93704-52:
(7*9)+(6*3)+(5*7)+(4*0)+(3*4)+(2*5)+(1*2)=140
140 % 10 = 0
So 93704-52-0 is a valid CAS Registry Number.

93704-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methyl-1H-indol-3-ylamine

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:93704-52-0 SDS

93704-52-0Upstream product

93704-52-0Relevant articles and documents

Synthesis of Substituted Indolobenzodiazepine Derivatives

Hiremath, Shivayogi P.,Hiremath, Dakshayani M.,Purohit, Muralidhar G.

, p. 930 - 933 (2007/10/02)

Various substituted-7,12-dihydroindolobenzodiazepines (4a-e) have been prepared from the corresponding 3-aminoindoles (1a-e) through Ullmann reaction with o-chloroaniline, acylation of the resulting 3-(o-aminophenylamino)indoles (2a-e) and cyclization of amides (3a-e) with POCl3.Similar systems have also been synthesized from ethyl 3-bromoindole-2-carboxylates (6a-e).The bromo esters react with o-phenylenediamine to give ethyl 3-(o-aminophenylamino)indole-2-carboxylates (7a-e) which undergo cyclization in the presence of PPA to yield 5,6,7,12-tetrahydroindolobenzodiazepin-6-ones (8a-e).

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