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CAS

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433728-73-5

2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 433728-73-5 Structure

  • Basic information

    1. Product Name: 2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE
    2. Synonyms: 2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE
    3. CAS NO:433728-73-5
    4. Molecular Formula: C18H23N3O
    5. Molecular Weight: 297.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 433728-73-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 505.502°C at 760 mmHg
    3. Flash Point: 259.518°C
    4. Appearance: /
    5. Density: 1.092g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.575
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE(433728-73-5)
    12. EPA Substance Registry System: 2-(4-AMINO-3-PYRIDINYL) N,N-BIS(1-METHYLETHYL)-BENZAMIDE(433728-73-5)

  • 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: 433728-73-5(Hazardous Substances Data)

433728-73-5 Usage

Chemical structure

The compound has a benzamide core structure with an amino-pyridinyl group and two isopropyl substituents.

Biological activities

The compound has reported anti-inflammatory and antiproliferative properties.

Potential therapeutic applications

The compound has been studied for its potential in treating various diseases, including cancer and inflammatory conditions.

Ongoing research

Further research is being conducted on the pharmacological properties and potential therapeutic applications of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 433728-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,7,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 433728-73:
(8*4)+(7*3)+(6*3)+(5*7)+(4*2)+(3*8)+(2*7)+(1*3)=155
155 % 10 = 5
So 433728-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N3O/c1-12(2)21(13(3)4)18(22)15-8-6-5-7-14(15)16-11-20-10-9-17(16)19/h5-13H,1-4H3,(H2,19,20)

433728-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-amino-3-pyridyl)-N,N-diisopropyl-benzamide

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:433728-73-5 SDS

433728-73-5Relevant articles and documents

Compounds and their use

-

, (2008/06/13)

This invention relates to compounds, pharmaceutical compositions, and methods of using the disclosed compounds for inhibiting PARP.

Design and synthesis of poly ADP-ribose polymerase-1 inhibitors. 2. Biological evaluation of aza-5[H]-phenanthridin-6-ones as potent, aqueous-soluble compounds for the treatment of ischemic injuries

Ferraris, Dana,Ko, Yao-Sen,Pahutski, Thomas,Ficco, Rica Pargas,Serdyuk, Larisa,Alemu, Christina,Bradford, Chadwick,Chiou, Tiffany,Hoover, Randall,Huang, Shirley,Lautar, Susan,Liang, Shi,Lin, Qian,Lu, May X.-C.,Mooney, Maria,Morgan, Lisa,Qian, Yongzhen,Tran, Scott,Williams, Lawrence R.,Wu, Qi Yi,Zhang, Jie,Zou, Yinong,Kalish, Vincent

, p. 3138 - 3151 (2007/10/03)

A series of aza-5[H]-phenanthridin-6-ones were synthesized and evaluated as inhibitors of poly ADP-ribose polymerase-1 (PARP-1). Inhibitory potency of the unsubstituted aza-5[H]-phenanthridin-6-ones (i.e., benzonaphthyridones) was dependent on the positio

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