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1-Pyridin-3-ylpropan-1-amine, also known as 3-(1-Pyrrolidinyl)propylamine, is a chemical compound characterized by a molecular formula of C8H12N2. It features a pyridine ring connected to a propan-1-amine group, which endows it with unique structural and reactive properties. 1-Pyridin-3-ylpropan-1-amine is pivotal in the realm of organic chemistry and drug development, serving as a versatile intermediate in the synthesis of pharmaceuticals and other organic compounds. Its potential in therapeutic drug development is attributed to its capacity to engage with biological targets within the body, making it a promising candidate for various applications.

60289-67-0

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60289-67-0 Usage

Uses

Used in Pharmaceutical Synthesis:
1-Pyridin-3-ylpropan-1-amine is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new therapeutic agents. Its unique structure allows it to form part of complex molecular frameworks that can target specific biological pathways, thereby enhancing the efficacy of resulting drugs.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 1-Pyridin-3-ylpropan-1-amine is employed as an intermediate for the preparation of a variety of organic compounds. Its reactivity and structural features make it suitable for creating diverse chemical entities with potential applications in different industries.
Used in Research and Development Laboratories:
1-Pyridin-3-ylpropan-1-amine plays a significant role in research and development settings, where it is used in the preparation of various chemical substances. Its presence in laboratories underscores its importance in advancing scientific knowledge and facilitating the discovery of novel compounds with practical applications.
Overall, 1-Pyridin-3-ylpropan-1-amine's multifaceted applications across pharmaceuticals, organic chemistry, and research and development highlight its indispensable nature in the creation and understanding of new chemical entities and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 60289-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60289-67:
(7*6)+(6*0)+(5*2)+(4*8)+(3*9)+(2*6)+(1*7)=130
130 % 10 = 0
So 60289-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-2-8(9)7-4-3-5-10-6-7/h3-6,8H,2,9H2,1H3

60289-67-0 Well-known Company Product Price

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  • Aldrich

  • (CBR00143)  1-(3-Pyridinyl)-1-propanamine  AldrichCPR

  • 60289-67-0

  • CBR00143-1G

  • 3,221.01CNY

  • Detail

60289-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyridin-3-ylpropan-1-amine

1.2 Other means of identification

Product number -
Other names 1-pyridin-3-yl-propylamine

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:60289-67-0 SDS

60289-67-0Relevant academic research and scientific papers

ORGANIC COMPOUNDS

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Page/Page column 37, (2010/03/02)

The present invention relates to compounds of formula (I) wherein X, R1, R2, R3, R4 and R5 are as defined herein, which are useful for treating diseases which respond to CXCR2 receptor mediators. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

Anthranilamides and methods of their use

-

, (2008/06/13)

The present invention is related to anthranilamides of formula I, in which R(1) to R(7) have the meanings indicated herein, a process for their preparation, their use as medicaments, and pharmaceutical preparations containing them. The compounds act on the Kv1.5 potassium channel and inhibit a potassium current which is referred to as the ultra-rapidly activating delayed rectifier in the atrium of the human heart. The compounds are therefore suitable for use as novel antiarrhythmic agents for the treatment and prophylaxis of atrial arrhythmias (e.g., atrial fibrillation (AF) or atrial flutter).

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