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  • 7346-79-4 Structure
  • Basic information

    1. Product Name: cyclohexylammonium acetate
    2. Synonyms: cyclohexylammonium acetate;CYCLOHEXYLAMINE,ACETATE
    3. CAS NO:7346-79-4
    4. Molecular Formula: C2H4O2*C6H13N
    5. Molecular Weight: 159.22608
    6. EINECS: 230-871-4
    7. Product Categories: N/A
    8. Mol File: 7346-79-4.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 134.5°C at 760 mmHg
    3. Flash Point: 32.2°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 8.07mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: cyclohexylammonium acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: cyclohexylammonium acetate(7346-79-4)
    12. EPA Substance Registry System: cyclohexylammonium acetate(7346-79-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7346-79-4(Hazardous Substances Data)

7346-79-4 Usage

Description

Cyclohexylammonium acetate is a chemical compound consisting of cyclohexylammonium cations and acetate anions, commonly utilized as a phase-transfer catalyst to facilitate the transfer of reactants between immiscible phases in chemical reactions.

Uses

Used in Organic Synthesis:
Cyclohexylammonium acetate is used as a phase-transfer catalyst for facilitating the synthesis of various organic compounds, particularly in reactions involving quaternary ammonium salts, due to its effectiveness in aiding reactant transfer.
Used in Pharmaceutical Production:
In the pharmaceutical industry, cyclohexylammonium acetate is used as a reagent in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, cyclohexylammonium acetate is employed as a reagent in the synthesis of agrochemicals, playing a role in the development of products for agricultural applications.
Used in Coatings and Adhesives Formulation:
Cyclohexylammonium acetate is used as a component in the formulation of certain types of coatings and adhesives, enhancing their properties and performance.
Used in Corrosion Inhibition:
In industrial processes, cyclohexylammonium acetate has shown potential as a corrosion inhibitor, helping to protect materials from degradation and extending their service life.

Check Digit Verification of cas no

The CAS Registry Mumber 7346-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7346-79:
(6*7)+(5*3)+(4*4)+(3*6)+(2*7)+(1*9)=114
114 % 10 = 4
So 7346-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N.C2H4O2/c7-6-4-2-1-3-5-6;1-2(3)4/h6H,1-5,7H2;1H3,(H,3,4)

7346-79-4SDS

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 Acetic acid.cyclohexanamine

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:7346-79-4 SDS

7346-79-4Upstream product

7346-79-4Relevant articles and documents

NOVEL MULTIMERIC MOLECULES, A PROCESS FOR PREPARING THE SAME AND THE USE THEREOF FOR MANUFACTURING MEDICINAL DRUGS

-

, (2010/06/16)

The invention relates to a compound of the formula (I): in which k and j are independently 0 or 1, Y is a macrocycle in which the cycle includes 9 to 36 carbon atoms and is functionalised by three amino functions and by a chain for attaching the spacer arm Z via an X bond, Rc is a binding pattern with a receptor of the TNF superfamily, X is a chemical function for binding the Y group to the space arm, and Z is a bi-, tri- or tetra-functional spacer arm.

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