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1-Pyridin-2-ylmethyl-[1,4]diazepane, a heterocyclic compound with the molecular formula C13H20N2, features a central six-membered ring with two nitrogen atoms and a pyridine ring attached to one of the carbon atoms. 1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE has potential pharmacological activity and is of interest in medicinal chemistry due to its unique structure and potential applications in the treatment of neurological disorders, coordination chemistry, and the synthesis of other organic compounds.

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  • 247118-06-5 Structure
  • Basic information

    1. Product Name: 1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE
    2. Synonyms: BUTTPARK 82\12-43;CHEMBRDG-BB 4004617;1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE;AKOS BBV-014109;UKRORGSYN-BB BBV-014109;1-(pyridin-2-ylmethyl)-1,4-diazepane(SALTDATA: 3tosilate)
    3. CAS NO:247118-06-5
    4. Molecular Formula: C11H17N3
    5. Molecular Weight: 191.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247118-06-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 294.9°C at 760 mmHg
    3. Flash Point: 132.2°C
    4. Appearance: /
    5. Density: 1.046g/cm3
    6. Vapor Pressure: 0.00157mmHg at 25°C
    7. Refractive Index: 1.538
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.43±0.20(Predicted)
    11. CAS DataBase Reference: 1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE(247118-06-5)
    13. EPA Substance Registry System: 1-PYRIDIN-2-YLMETHYL-[1,4]DIAZEPANE(247118-06-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 247118-06-5(Hazardous Substances Data)

247118-06-5 Usage

Uses

Used in Pharmaceutical Industry:
1-Pyridin-2-ylmethyl-[1,4]diazepane is used as a potential therapeutic agent for the treatment of various neurological disorders, leveraging its pharmacological properties to address specific conditions.
Used in Coordination Chemistry:
1-Pyridin-2-ylmethyl-[1,4]diazepane serves as a ligand in coordination chemistry, contributing to the formation of metal complexes that may have unique properties and applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-Pyridin-2-ylmethyl-[1,4]diazepane is utilized as a building block or intermediate in the synthesis of other organic compounds, potentially leading to the development of new pharmaceuticals or chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 247118-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,1,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 247118-06:
(8*2)+(7*4)+(6*7)+(5*1)+(4*1)+(3*8)+(2*0)+(1*6)=125
125 % 10 = 5
So 247118-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N3/c1-2-6-13-11(4-1)10-14-8-3-5-12-7-9-14/h1-2,4,6,12H,3,5,7-10H2

247118-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(pyridin-2-ylmethyl)-1,4-diazepane

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:247118-06-5 SDS

247118-06-5Downstream Products

247118-06-5Relevant articles and documents

Ferromagnetic coupling in a unique Cu(II) metallacyclophane with functionalized diazamesocyclic ligands formed by Cu(II)-directed self-assembly: Magneto-structural correlations for dichloro-bridged Cu(II) dinuclear complexes

Du, Miao,Guo, Ya-Mei,Bu, Xian-He,Ribas, Joan,Monfort, Montserrat

, p. 645 - 650 (2002)

Two new di-μ-Cl dinuclear CuII complexes [Cu(HL1)Cl2]2(ClO4)2 (1) and [Cu2(L2)2Cl2](ClO4) 2 (2) with the pyridyl-functionalized diazamesocyclic ligands 1,5-bis(pyridin-4-ylmethyl)-1,5-diazacyclooctane (L1) and 1-(pyridin-2-ylmethyl)-1,4-diazacycloheptane (L2) have been synthesized and structurally characterized by single crystal X-ray diffraction. Complex 1 is a unique paramagnetic CuII metallamacrocycle (ca. 14.1 × 3.5 A 2) directly self-assembled by metal ions and the organic spacer under strongly acidic conditions. The magnetic properties of both complexes have been investigated by variable-temperature magnetic susceptibility measurements. Although complexes 1 and 2 have almost the same geometrical parameters for CuII, their magnetic parameters vary from ferromagnetic for 1 to antiferromagnetic for 2. The magneto-structural correlation of such complexes has been further developed.

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