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84145-72-2

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84145-72-2 Usage

Description

4-Cyanopentylmorpholine is a chemical compound with the molecular formula C10H18N2O and a molecular weight of 182.26 g/mol. It is a liquid that is used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceuticals. This morpholine derivative features a cyano group attached to a pentyl chain, making it a versatile intermediate in the production of pharmaceuticals and agrochemicals. Additionally, it can serve as a solvent or a chemical reagent in organic synthesis, highlighting its importance across various industrial applications.

Uses

Used in Pharmaceutical Industry:
4-Cyanopentylmorpholine is used as a building block for the synthesis of various drugs and pharmaceuticals, contributing to the development of new medications and therapies.
Used in Agrochemical Production:
4-cyanopentylmorpholine is utilized as an intermediate in the production of agrochemicals, playing a role in the creation of products that protect and enhance crop yields.
Used as a Solvent:
4-Cyanopentylmorpholine is used as a solvent in organic synthesis, facilitating chemical reactions and aiding in the production of various organic compounds.
Used as a Chemical Reagent:
In organic synthesis, 4-cyanopentylmorpholine serves as a chemical reagent, enabling specific chemical transformations and the synthesis of target molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 84145-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84145-72:
(7*8)+(6*4)+(5*1)+(4*4)+(3*5)+(2*7)+(1*2)=132
132 % 10 = 2
So 84145-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O/c10-4-2-1-3-5-11-6-8-12-9-7-11/h1-3,5-9H2

84145-72-2SDS

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 5-morpholin-4-ylpentanenitrile

1.2 Other means of identification

Product number -
Other names 4-cyanopentylmorpholine

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:84145-72-2 SDS

84145-72-2Relevant articles and documents

Solid state and solution study on the formation of inorganic anion complexes with a series of tetrazine-based ligands

Savastano, Matteo,García-Gallarín, Celeste,Giorgi, Claudia,Gratteri, Paola,de la Torre, Maria Dolores López,Bazzicalupi, Carla,Bianchi, Antonio,Melguizo, Manuel

, (2019/06/20)

Four molecules (L1–L4) constituted by an s-tetrazine ring appended with two identical aliphatic chains of increasing length bearing terminal morpholine groups were studied as anion receptors in water. The basicity properties of these molecules were also investigated. Speciation of the anion complexes formed in solution and determination of their stability constants were performed by means of potentiometric (pH-metric) titrations, while further information was obtained by NMR and isothermal titration calorimetry (ITC) measurements. The crystal structures of two neutral ligands (L3, L4) and of their H2L3(ClO4)2·2H2O, H2L4(ClO4)2·2H2O, H2L3(PF6)2, and H2L3(PF6)2·2H2O anion complexes were determined by single crystal X-ray diffraction. The formation of anion–π interactions is the leitmotiv of these complexes, both in solution and in the solid state, although hydrogen bonding and/or formation of salt-bridges can contribute to their stability. Evidence of the ability of these ligands to form anion–π interactions is given by the observation that even the neutral (not-protonated) molecules bind anions in water to form complexes of significant stability, including elusive OH? anions.

BENZYL SUBSTITUTED INDAZOLES

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Page/Page column 256; 257, (2016/04/10)

Compounds of formula (I) and their use as pharmaceuticals.

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