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2-Pyridinamine, N-(diphenylmethylene)-3-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 628322-77-0 Structure
  • Basic information

    1. Product Name: 2-Pyridinamine, N-(diphenylmethylene)-3-fluoro-
    2. Synonyms:
    3. CAS NO:628322-77-0
    4. Molecular Formula: C18H13FN2
    5. Molecular Weight: 276.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 628322-77-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Pyridinamine, N-(diphenylmethylene)-3-fluoro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyridinamine, N-(diphenylmethylene)-3-fluoro-(628322-77-0)
    11. EPA Substance Registry System: 2-Pyridinamine, N-(diphenylmethylene)-3-fluoro-(628322-77-0)
  • 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: 628322-77-0(Hazardous Substances Data)

628322-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 628322-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 628322-77:
(8*6)+(7*2)+(6*8)+(5*3)+(4*2)+(3*2)+(2*7)+(1*7)=160
160 % 10 = 0
So 628322-77-0 is a valid CAS Registry Number.

628322-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name benzhydrylidene(3-fluoropyridin-2-yl)amine

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:628322-77-0 SDS

628322-77-0Downstream Products

628322-77-0Relevant articles and documents

8-Fluoroimidazo[1,2-a]pyridine: Synthesis, physicochemical properties and evaluation as a bioisosteric replacement for imidazo[1,2-a]pyrimidine in an allosteric modulator ligand of the GABAA receptor

Humphries, Alexander C.,Gancia, Emanuela,Gilligan, Myra T.,Goodacre, Simon,Hallett, David,Merchant, Kevin J.,Thomas, Steve R.

, p. 1518 - 1522 (2006)

8-Fluoroimidazo[1,2-a]pyridine has been established as a physicochemical mimic of imidazo[1,2-a]pyrimidine, using both in silico and traditional techniques. Furthermore, a novel synthesis of a 3,7-disubstituted-8- fluoroimidazopyridine 3 has been developed and the utility of the physicochemical mimicry has been demonstrated in an in vitro system. Here, the 8-fluoroimidazopyridine ring contained in ligand 3 acts as a bioisosteric replacement for imidazopyrimidine in the GABAA receptor modulator 2.

IMIDAZO-PYRIDINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS

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Page 43, (2010/02/04)

A class of 8-fluoro-3-phenylimidazo[1,2-a]pyridine derivatives, substituted at the meta position of the phenyl ring by an optionally substituted aryl or heteroaryl group, or by a pyrrolidinonyl group, which is directly attached or bridged by an oxygen atom or by a -NH- or -OCH2- linkage, being selective ligands for GABAA receptors, in particular having high affinity for the α2 and/or α3 and/or α5 subunit thereof, are accordingly of benefit in the treatment and/or prevention of adverse conditions of the central nervous system, including anxiety, convulsions and cognitive disorders.

8-FLUORIMIDAZO`1,2-A!PYRIDINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS

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Page 35-36, (2010/02/04)

A class of 8-fluoroimidazo[1,2-a]pyridine derivatives, substituted at the 3-position by an optionally substituted five-membered or six-membered heteroaromatic ring, being selective ligands for GABAA receptors, in particular having high affinity for the α2 and/or α3 and/or α5 subunit thereof, are accordingly of benefit in the treatment and/or prevention of adverse conditions of the central nervous system, including anxiety, convulsions and cognitive disorders.

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