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449173-27-7

4-Pyridinamine, 3-(1-propynyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 449173-27-7 Structure

  • Basic information

    1. Product Name: 4-Pyridinamine, 3-(1-propynyl)- (9CI)
    2. Synonyms: 4-Pyridinamine, 3-(1-propynyl)- (9CI);3-(prop-1-ynyl)pyridin-4-amine
    3. CAS NO:449173-27-7
    4. Molecular Formula: C8H8N2
    5. Molecular Weight: 132.16252
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 449173-27-7.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: 4-Pyridinamine, 3-(1-propynyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Pyridinamine, 3-(1-propynyl)- (9CI)(449173-27-7)
    11. EPA Substance Registry System: 4-Pyridinamine, 3-(1-propynyl)- (9CI)(449173-27-7)

  • 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: 449173-27-7(Hazardous Substances Data)

449173-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 449173-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,1,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 449173-27:
(8*4)+(7*4)+(6*9)+(5*1)+(4*7)+(3*3)+(2*2)+(1*7)=167
167 % 10 = 7
So 449173-27-7 is a valid CAS Registry Number.

449173-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-1-ynylpyridin-4-ylamine

1.2 Other means of identification

Product number -
Other names 3-prop-1-yn-1-ylpyridin-4-amine

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:449173-27-7 SDS

449173-27-7Relevant articles and documents

PROTEASOME ACTIVITY ENHANCING COMPOUNDS

-

Page/Page column 157-158, (2015/06/03)

The present invention is directed to compounds having the Formula (I), (II), (III), (IV), and (V), compositions thereof, the methods of synthesis of the compouds of interest, and to methods for the treatment of a condition associated with a dysfunction in proteostasis, such as cancer, inflammatory conditions, neurodegeneration, metabolic conditions, comprising administering an effective amount of a compound of the invention.

Synthesis of novel heteroaromatics structurally related to ellipticine alkaloids via thermolysis of pyridannulated enyne-carbodiimides

Lu, Xiaoling,Petersen, Jeffrey L.,Wang, Kung K.

, p. 5412 - 5415 (2007/10/03)

New synthetic pathways to the 5H-pyrido[3',4':4,5]pyrrolo[2,3-b]quinolines 6, the 6H-pyrido[3',4':4,5]pyrrolo[2,3-b] [1,6]naphthyridines 7, and the 11H-pyrido[43,3': 4,5]pyrrolo[2,3-b]quinolines 8 via thermolysis of the pyridannulated enyne-carbodiimides 14, 19, and 23 were established. These novel heteroaromatic systems are structurally related to ellipticine alkaloids and could serve as DNA- intercalating agents.

Transition metal catalyzed synthesis of 5-azaindoles

Xu, Lianhong,Lewis, Iestyn R.,Davidsen, Steven K.,Summers, James B.

, p. 5159 - 5162 (2007/10/03)

In an effort to develop synthetic procedures for the preparation of 2- substituted 5-azaindoles, the synthesis and cyclization reactions of acetylenic aminopyridines was explored. A novel method for the synthesis of 2-substituted 5-azaindoles via a transi

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