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106795-72-6

1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106795-72-6 Structure

  • Basic information

    1. Product Name: 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE
    2. Synonyms: 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE;1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE 95%;1-(2-Fluorophenyl)cyclohexanecarbonitrile,95%;CYCLOHEXANECARBONITRILE, 1-(2-FLUOROPHENYL)-;1-(2-fluorophenyl)cyclohexane-1-carbonitrile
    3. CAS NO:106795-72-6
    4. Molecular Formula: C13H14FN
    5. Molecular Weight: 203.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106795-72-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 326.7°Cat760mmHg
    3. Flash Point: 141°C
    4. Appearance: /
    5. Density: 1.0708 (estimate)
    6. Vapor Pressure: 0.000212mmHg at 25°C
    7. Refractive Index: 1.5195-1.522
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE(106795-72-6)
    12. EPA Substance Registry System: 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE(106795-72-6)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 36/37/38-20/21/22
    3. Safety Statements: 36/37/39-26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 106795-72-6(Hazardous Substances Data)

106795-72-6 Usage

Chemical Properties

Clear colorless to brown liquid

Check Digit Verification of cas no

The CAS Registry Mumber 106795-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,9 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106795-72:
(8*1)+(7*0)+(6*6)+(5*7)+(4*9)+(3*5)+(2*7)+(1*2)=146
146 % 10 = 6
So 106795-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H14FN/c14-12-7-3-2-6-11(12)13(10-15)8-4-1-5-9-13/h2-3,6-7H,1,4-5,8-9H2

106795-72-6SDS

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 1-(2-fluorophenyl)cyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-(2-FLUOROPHENYL)CYCLOHEXANECARBONITRILE

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:106795-72-6 SDS

106795-72-6Relevant articles and documents

Process for preparing 3,3-disubstituted oxindoles and thio-oxindoles

-

Page/Page column 18, (2008/06/13)

Methods for preparing oxindole and thio-oxindole compounds are provided, which compounds are useful as precursors to useful pharmaceutical compounds. Specifically provided are methods for preparing 5-pyrrole-3,3-oxindole compounds and 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile. Also provided are methods for preparing iminobenzo[b]thiophene and benzo[b]thiophenone compounds.

Two New Oxindole Syntheses

Fleming, Ian,Loreto, Maria Antonietta,Wallace, Ian H.M.,Michael, Joseph P.

, p. 349 - 360 (2007/10/02)

Two oxindole syntheses are described, both starting from ketones, in which the carbonyl carbon becomes C-3 of the oxindole.The first route uses o-lithioformanilide followed by attack with cyanide ion and hydrolysis.The second uses a pinacol-type rearragement (or the γ-silyl alcohol variation) to create the quaternary centre, and involves an intramolecular displacement of fluoride ion from an unactivated benzene ring by an amide nitrogen to complete the lactam ring.The two routes are stereochemically complementary, giving different spiro-oxindoles from norbornanone.

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