Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-Pyridin-2-yl-ethylamine, also known as beta-phenylethylamine, is a chemical compound with the molecular formula C8H11N. It is a derivative of phenethylamine and is recognized for its potential therapeutic effects on the central nervous system, where it modulates neurotransmitter levels. 1-PYRIDIN-2-YL-ETHYLAMINE is also known for its psychoactive properties, classifying it as a stimulant drug. Furthermore, it finds use in the production of agricultural chemicals, dyes, and pigments, showcasing its versatility in both pharmaceutical and industrial applications.

42088-91-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 42088-91-5 Structure
  • Basic information

    1. Product Name: 1-PYRIDIN-2-YL-ETHYLAMINE
    2. Synonyms: 1-PYRIDIN-2-YL-ETHYLAMINE;1-(2-Pyridyl)ethylamine;2-(1-Aminoethyl)pyridine;1-Pyridin-2-yl-ethylamine oxalate;1-(2-Pyridyl)ethaneamine;1-(2-Pyridinyl)ethylamine;1-Pyridine-2-yl-ethylamine;2-Pyridinemethanamine, .alpha.-methyl-
    3. CAS NO:42088-91-5
    4. Molecular Formula: C7H10N2
    5. Molecular Weight: 122.17
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 42088-91-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 194.5 °C at 760 mmHg
    3. Flash Point: 78℃
    4. Appearance: /
    5. Density: 1.002 g/mL at 25 °C
    6. Vapor Pressure: 0.44mmHg at 25°C
    7. Refractive Index: n20/D1.528
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: 9.05±0.39(Predicted)
    11. Sensitive: Air Sensitive
    12. CAS DataBase Reference: 1-PYRIDIN-2-YL-ETHYLAMINE(CAS DataBase Reference)
    13. NIST Chemistry Reference: 1-PYRIDIN-2-YL-ETHYLAMINE(42088-91-5)
    14. EPA Substance Registry System: 1-PYRIDIN-2-YL-ETHYLAMINE(42088-91-5)
  • Safety Data

    1. Hazard Codes: T,Xi
    2. Statements: 25-37/38-41
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: UN2735
    5. WGK Germany: nwg
    6. RTECS:
    7. HazardClass: 8
    8. PackingGroup: III
    9. Hazardous Substances Data: 42088-91-5(Hazardous Substances Data)

42088-91-5 Usage

Uses

Used in Pharmaceutical Synthesis:
1-Pyridin-2-yl-ethylamine is used as a precursor in the synthesis of various pharmaceuticals and biologically active compounds, leveraging its ability to modulate neurotransmitter levels in the brain for potential therapeutic benefits.
Used in Central Nervous System Applications:
In the field of neuroscience, 1-Pyridin-2-yl-ethylamine is utilized for its potential therapeutic effects on the central nervous system, where it can influence neurotransmitter levels, offering possible treatments for neurological conditions.
Used in Psychoactive Drug Development:
Due to its psychoactive properties, 1-Pyridin-2-yl-ethylamine is used in the development of stimulant drugs, contributing to the advancement of medications targeting cognitive function and mood regulation.
Used in Agricultural Chemical Production:
1-Pyridin-2-yl-ethylamine is employed as a key component in the production of agricultural chemicals, where it may contribute to the development of more effective and targeted crop protection agents.
Used in Dyes and Pigments Industry:
In the dyes and pigments industry, 1-Pyridin-2-yl-ethylamine is used for its ability to create a range of colors and shades, enhancing the variety and quality of products available for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 42088-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,8 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42088-91:
(7*4)+(6*2)+(5*0)+(4*8)+(3*8)+(2*9)+(1*1)=115
115 % 10 = 5
So 42088-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2/c1-6(8)7-4-2-3-5-9-7/h2-6H,8H2,1H3/p+1/t6-/m1/s1

42088-91-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H26046)  1-(2-Pyridyl)ethylamine, 96%   

  • 42088-91-5

  • 250mg

  • 2234.0CNY

  • Detail
  • Alfa Aesar

  • (H26046)  1-(2-Pyridyl)ethylamine, 96%   

  • 42088-91-5

  • 1g

  • 6370.0CNY

  • Detail
  • Aldrich

  • (724939)  2-(1-Aminoethyl)pyridine  97%

  • 42088-91-5

  • 724939-500MG

  • 1,100.97CNY

  • Detail

42088-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Pyridin-2-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 1-PYRIDIN-2-YL-ETHYLAMINE

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:42088-91-5 SDS

42088-91-5Relevant articles and documents

Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono- and di-amine transaminases

Galman, James L.,Slabu, Iustina,Weise, Nicholas J.,Iglesias, Cesar,Parmeggiani, Fabio,Lloyd, Richard C.,Turner, Nicholas J.

supporting information, p. 361 - 366 (2017/08/14)

The discovery and characterisation of enzymes with both monoamine and diamine transaminase activity is reported, allowing conversion of a wide range of target ketone substrates with just a small excess of amine donor. The diamine co-substrates (putrescine, cadaverine or spermidine) are bio-derived and the enzyme system results in very little waste, making it a greener strategy for the production of valuable amine fine chemicals and pharmaceuticals.

But-2-ene-1,4-diamine and But-2-ene-1,4-diol as Donors for Thermodynamically Favored Transaminase- and Alcohol Dehydrogenase-Catalyzed Processes

Martínez-Montero, Lía,Gotor, Vicente,Gotor-Fernández, Vicente,Lavandera, Iván

supporting information, p. 1618 - 1624 (2016/10/13)

Both cis- and trans-but-2-ene-1,4-diamines have been prepared and efficiently applied as sacrificial cosubstrates in enzymatic transamination reactions. The best results were obtained with the cis-diamine. The thermodynamic equilibrium of the stereoselective transamination process is shifted to the amine formation due to tautomerization of 5H-pyrrole into 1H-pyrrole, achieving high conversions (78–99%) and enantiomeric excess (up to >99%) by using a small excess of the amine donor. Furthermore, when the reaction proceeded, a strong coloration was observed due to polymerization of 1H-pyrrole. A structurally related compound, cis-but-2-ene-1,4-diol, has been utilized as cosubstrate in different alcohol dehydrogenase (ADH)-mediated bioreductions. In this case, high conversions (91–99%) were observed due to a lactonization process. Both strategies are convenient from both synthetic and atom economy points of view in the production of valuable optically active products. (Figure presented.).

Voltammetric, potentiometric and spectrophotometric studies of some hydrazones and their metal complexes in ethanolic-aqueous buffered solutions

Ghoneim, Mohammed M.,El-Hallag, Ibrahim S.,El-Baradie, Kamal Y.,El-Desoky, Hanaa S.,El-Attar, Mona A.

, p. 285 - 299 (2007/10/03)

The electrochemical behavior of some hydrazones derived from 6-chloro-2-hydrazinopyridine in the Britton-Robinson universal buffer of pH 2-11 containing 35% ethanol was investigated at the mercury electrode using dc-polarography, controlled-potential coulometry, and cyclic voltammetry techniques. The examined hydrazones were reduced in solutions of pH 2 single bond. The mechanistic pathway of the electrode reaction of the studied compounds was elucidated and discussed. The pK a values of the examined hydrazones and the stoichiometry of their complexes in solution with some transition metal ions were determined spectrophotometrically. The dissociation constants and the thermodynamic parameters of the investigated hydrazones, and the stability constants of their metal complexes in solution were determined potentiometrically. Springer-Verlag 2006.

PYRAZOLE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSYNE KINASES

-

Page/Page column 98, (2008/06/13)

Compounds of formula (I): and their use in the inhibition of Trk activity are described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 42088-91-5