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CAS

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7175-49-7

N-Ethyldicyclohexylamine is a clear colorless liquid that is utilized in the synthesis of various products, including F-amines. It is formed through a process involving incomplete fluorination and fragmentation reactions, making it a valuable compound in the chemical industry.

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  • 7175-49-7 Structure

  • Basic information

    1. Product Name: N-ETHYLDICYCLOHEXYLAMINE
    2. Synonyms: N-ETHYLDICYCLOHEXYLAMINE;N,N-DICYCLOHEXYLETHYLAMINE;Cyclohexanamine, N-cyclohexyl-N-ethyl-;Dicyclohexylamine, N-ethyl-;n-cyclohexyl-n-ethyl-cyclohexanamin;N-Cyclohexyl-N-ethylcyclohexanamine;n-ethyl-dicyclohexylamin;N-cyclohexyl-N-ethylcyclohexylamine
    3. CAS NO:7175-49-7
    4. Molecular Formula: C14H27N
    5. Molecular Weight: 209.37
    6. EINECS: 230-534-1
    7. Product Categories: Amines;Building Blocks;C14 to C16;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks
    8. Mol File: 7175-49-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 114-115 °C3 mm Hg(lit.)
    3. Flash Point: >230 °F
    4. Appearance: Clear colorless/Liquid
    5. Density: 0.91 g/mL at 20 °C(lit.)
    6. Vapor Pressure: 0.00507mmHg at 25°C
    7. Refractive Index: n20/D 1.485(lit.)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 11.11±0.20(Predicted)
    11. BRN: 2240256
    12. CAS DataBase Reference: N-ETHYLDICYCLOHEXYLAMINE(CAS DataBase Reference)
    13. NIST Chemistry Reference: N-ETHYLDICYCLOHEXYLAMINE(7175-49-7)
    14. EPA Substance Registry System: N-ETHYLDICYCLOHEXYLAMINE(7175-49-7)

  • Safety Data

    1. Hazard Codes: C
    2. Statements: 34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: UN 2735 8/PG 2
    5. WGK Germany: 3
    6. RTECS: HY4150000
    7. HazardClass: 8
    8. PackingGroup: III
    9. Hazardous Substances Data: 7175-49-7(Hazardous Substances Data)

7175-49-7 Usage

Uses

Used in Chemical Synthesis:
N-Ethyldicyclohexylamine is used as a chemical intermediate for the synthesis of F-amines and other products. Its unique structure and properties allow it to participate in various chemical reactions, contributing to the formation of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-Ethyldicyclohexylamine is used as a building block for the development of new drugs. Its versatility in chemical reactions enables the creation of diverse molecular structures with potential therapeutic applications.
Used in Material Science:
N-Ethyldicyclohexylamine is also employed in material science, where it can be used to develop new materials with specific properties. Its ability to undergo various chemical reactions allows for the creation of materials with tailored characteristics for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7175-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7175-49:
(6*7)+(5*1)+(4*7)+(3*5)+(2*4)+(1*9)=107
107 % 10 = 7
So 7175-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H27N/c1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h13-14H,2-12H2,1H3/p+1

7175-49-7SDS

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 N-cyclohexyl-N-ethylcyclohexanamine

1.2 Other means of identification

Product number -
Other names N,N-Dicyclohexylethylamine

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:7175-49-7 SDS

7175-49-7Relevant articles and documents

Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid

Gupta, Surabhi,Sureshbabu, Popuri,Singh, Adesh Kumar,Sabiah, Shahulhameed,Kandasamy, Jeyakumar

supporting information, p. 909 - 913 (2017/02/15)

A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies.

Photocatalytic hydrodefluorination: Facile access to partially fluorinated aromatics

Senaweera, Sameera M.,Singh, Anuradha,Weaver, Jimmie D.

supporting information, p. 3002 - 3005 (2014/03/21)

Polyfluorinated aromatics are essential to materials science as well as the pharmaceutical and agrochemical industries and yet are often difficult to access. This Communication describes a photocatalytic hydrodefluorination approach which begins with easily accessible perfluoroarenes and selectively reduces the C-F bonds. The method allows facile access to a number of partially fluorinated arenes and takes place with unprecedented catalytic activity using a safe and inexpensive amine as the reductant.

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