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Pyridine,3-(1,1-difluoroethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114468-03-0 Structure
  • Basic information

    1. Product Name: Pyridine,3-(1,1-difluoroethyl)-(9CI)
    2. Synonyms: Pyridine,3-(1,1-difluoroethyl)-(9CI);3-(1,1-Difluoro-ethyl)-pyridine
    3. CAS NO:114468-03-0
    4. Molecular Formula: C7H7F2N
    5. Molecular Weight: 143.1339864
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 114468-03-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 168 °C
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.124±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.15±0.10(Predicted)
    10. CAS DataBase Reference: Pyridine,3-(1,1-difluoroethyl)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Pyridine,3-(1,1-difluoroethyl)-(9CI)(114468-03-0)
    12. EPA Substance Registry System: Pyridine,3-(1,1-difluoroethyl)-(9CI)(114468-03-0)
  • 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: 114468-03-0(Hazardous Substances Data)

114468-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114468-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114468-03:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*8)+(2*0)+(1*3)=110
110 % 10 = 0
So 114468-03-0 is a valid CAS Registry Number.

114468-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,1-Difluoroethyl)pyridine

1.2 Other means of identification

Product number -
Other names InChI=1/C7H7F2N/c1-7(8,9)6-3-2-4-10-5-6/h2-5H,1H

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:114468-03-0 SDS

114468-03-0Downstream Products

114468-03-0Relevant articles and documents

Deprotonative Functionalization of the Difluoromethyl Group

Bernier, David,Donnard, Morgan,Leroux, Frédéric R.,Panossian, Armen,Pazenok, Sergii,Santos, Laura,Vors, Jean-Pierre

, (2020)

The functionalization of 3-(difluoromethyl)pyridine has been developed via direct deprotonation of -CHF2 with a lithiated base and subsequent trapping with various electrophiles in THF. In situ quenching gives access to 3-pyridyl-CF2-SiMe2Ph as a new silylated compound, which can be postfunctionalized with a fluoride source to obtain a larger library of 3-(difluoroalkyl)pyridines that could not be accessed via direct deprotonation.

SUBSTITUTED AMIDE COMPOUNDS USEFUL AS FARNESOID X RECEPTOR MODULATORS

-

Page/Page column 134, (2020/08/28)

Disclosed are compounds of Formula (I): or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, wherein Q is: (i) halo, cyano, hydroxyl, NRxRx, C(O)OH, C(O)NH2, C1-6 alkyl substituted with zero to 6 R1a, or P(O)R1cR1c; or (ii) L R1; and A, X1, X2, X3, X4, Z1, Z2, R1, R1a, R1c, R2, R3a, R3b, Rx, L, a, b, and d are defined herein. Also disclosed are methods of using these compounds to modulate the activity of farnesoid X receptor (FXR); pharmaceutical compositions comprising these compounds; and methods of treating a disease, disorder, or condition associated with FXR dysregulation, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.

Syntheses of New Aromatic Compounds with Fluorinated Side Chains and their Chemical Reactivity

Haas, Alois,Spitzer, Martin,Lieb, Max

, p. 1329 - 1340 (2007/10/02)

The syntheses of a wide range of aromatic compounds of the type p-Y-C6H4CF2X(4-13) are described, and the chemical behavior of these compounds as a function of substituent Y is investigated .Analogously the pyridine derivatives 15, 17, and 18 were synthesized and characterized.From a correlation of the 19F-NMR data of these compounds with the Hammett constant of Y, participation of C-F ?-back-donation is seen as the cause for an observed shift of the 19F signals to lower field.

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