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2-N-(3-aminopropyl)-amino-5-bromopyridine, a chemical compound with the molecular formula C8H13BrN4, is a derivative of 5-bromopyridine featuring an amino group attached to the pyridine ring through a propyl linker. 2-N-(3-AMINOPROPYL)-AMINO-5-BROMOPYRIDINE is recognized for its unique structure and properties, making it a valuable intermediate in the synthesis of a variety of chemical compounds for pharmaceutical and agricultural applications.

92993-40-3

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92993-40-3 Usage

Uses

Used in Organic Synthesis:
2-N-(3-aminopropyl)-amino-5-bromopyridine is used as a building block in organic synthesis for the preparation of various biologically active compounds. Its versatile structure allows for the creation of a wide range of molecules with potential applications in different fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-N-(3-aminopropyl)-amino-5-bromopyridine is utilized as a key intermediate for the development of potential pharmaceutical agents. Its ability to be modified and incorporated into complex molecular structures contributes to the discovery of new drugs with specific therapeutic properties.
Used in Pharmaceutical Industry:
2-N-(3-aminopropyl)-amino-5-bromopyridine is used as a chemical intermediate for the synthesis of diverse pharmaceutical compounds. Its role in creating new drug candidates is crucial for advancing treatments and therapies for various diseases and conditions.
Used in Agrochemical Industry:
Similarly, in agrochemical applications, 2-N-(3-aminopropyl)-amino-5-bromopyridine serves as a building block for the development of agrochemicals. Its incorporation into these products can lead to the creation of more effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 92993-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,9 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92993-40:
(7*9)+(6*2)+(5*9)+(4*9)+(3*3)+(2*4)+(1*0)=173
173 % 10 = 3
So 92993-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12BrN3/c9-7-2-3-8(12-6-7)11-5-1-4-10/h2-3,6H,1,4-5,10H2,(H,11,12)

92993-40-3SDS

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 N'-(5-bromopyridin-2-yl)propane-1,3-diamine

1.2 Other means of identification

Product number -
Other names N-(3-aminopropyl)-5-bromopyridin-2-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:92993-40-3 SDS

92993-40-3Relevant academic research and scientific papers

Discovery of a novel non-peptide somatostatin agonist with SST4 selectivity

Ankersen, Michael,Crider, Michael,Liu, Shengquan,Ho, Bin,Andersen, Henrik S.,Stidsen, Carsten

, p. 1368 - 1373 (2007/10/03)

The discovery of novel non-peptide compounds with a high affinity for the peptide hormone somatostatin (SST) receptor is described. The compounds were tested for affinity at five human SST receptor subtypes individually expressed in mammalian cells. The c

Nonpeptide somatostatin agonists with sst4 selectivity: Synthesis and structure-activity relationships of thioureas

Liu, Shenquan,Tang, Cheng,Ho, Bin,Ankersen, Michael,Stidsen, Carsten E.,Crider, A. Michael

, p. 4693 - 4705 (2007/10/03)

Utilizing NNC 26-9100 (11) as a structural lead, a variety of nonpeptide derivatives of somatostatin were synthesized and evaluated for sst2 and sst4 receptor binding affinity. A novel thiourea scaffold was utilized to attach (1) a h

Pyridylaminoalkylaminopyrimidones useful as histamine H1 -antagonists

-

, (2008/06/13)

Pyridine derivatives are disclosed which are useful as histamine H1 -antagonists.

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