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360045-07-4

5-amino-1-(3,5-dimethylphenyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 360045-07-4 Structure

  • Basic information

    1. Product Name: 5-amino-1-(3,5-dimethylphenyl)-1H-indole
    2. Synonyms: 5-amino-1-(3,5-dimethylphenyl)-1H-indole
    3. CAS NO:360045-07-4
    4. Molecular Formula: C16H16N2
    5. Molecular Weight: 236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 360045-07-4.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: 5-amino-1-(3,5-dimethylphenyl)-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-amino-1-(3,5-dimethylphenyl)-1H-indole(360045-07-4)
    11. EPA Substance Registry System: 5-amino-1-(3,5-dimethylphenyl)-1H-indole(360045-07-4)

  • 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: 360045-07-4(Hazardous Substances Data)

360045-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360045-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,0,4 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 360045-07:
(8*3)+(7*6)+(6*0)+(5*0)+(4*4)+(3*5)+(2*0)+(1*7)=104
104 % 10 = 4
So 360045-07-4 is a valid CAS Registry Number.

360045-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-dimethylphenyl)indol-5-amine

1.2 Other means of identification

Product number -
Other names 1H-Indol-5-amine,1-(3,5-dimethylphenyl)

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:360045-07-4 SDS

360045-07-4Relevant articles and documents

Design and synthesis of subtype-selective cyclooxygenase (COX) inhibitors derived from thalidomide

Sano, Hiroko,Noguchi, Tomomi,Tanatani, Aya,Hashimoto, Yuichi,Miyachi, Hiroyuki

, p. 3079 - 3091 (2007/10/03)

A series of substituted indoline and indole derivatives with cyclooxygenase (COX)-inhibitory activity was prepared during our structural development studies based on thalidomide as a multi-template lead compound. Structure-activity relationship studies in

Expanding Pd-catalyzed C-N bond-forming processes: The first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions

Huang, Xiaohua,Anderson, Kevin W.,Zim, Danilo,Jiang, Lei,Klapars, Artis,Buchwald, Stephen L.

, p. 6653 - 6655 (2007/10/03)

The first general method for the Pd-catalyzed amination of aryl tosylates and benzenesulfonates was developed utilizing ligand 1, which belongs to a new generation of biaryl monophosphine ligands. In addition, the new catalyst system for the first time enables amidation of aryl arenesulfonates and aqueous amination protocols that do not necessitate the use of cosolvents. The substrate scope has been significantly expanded to include aryl halides containing primary amides and free carboxylic acid groups. In the case of multifunctional substrates, the Pd-catalyzed amination can provide selectivity that is complementary to the Cu-catalyzed C-N bond-forming processes. Copyright

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