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(4-fluorophenyl)(phenyl)methylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55095-26-6 Structure
  • Basic information

    1. Product Name: (4-fluorophenyl)(phenyl)methylamine
    2. Synonyms: (4-fluorophenyl)(phenyl)methylamine;4-FLUOROBENZHYDRYLAMINE;OTAVA-BB 1179198
    3. CAS NO:55095-26-6
    4. Molecular Formula: C13H12FN
    5. Molecular Weight: 201.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55095-26-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-fluorophenyl)(phenyl)methylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-fluorophenyl)(phenyl)methylamine(55095-26-6)
    11. EPA Substance Registry System: (4-fluorophenyl)(phenyl)methylamine(55095-26-6)
  • 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: 55095-26-6(Hazardous Substances Data)

55095-26-6 Usage

Synthesis Reference(s)

Synthesis, p. 667, 2000 DOI: 10.1055/s-2000-6391

Check Digit Verification of cas no

The CAS Registry Mumber 55095-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,9 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55095-26:
(7*5)+(6*5)+(5*0)+(4*9)+(3*5)+(2*2)+(1*6)=126
126 % 10 = 6
So 55095-26-6 is a valid CAS Registry Number.

55095-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name <(4-fluorophenyl)phenylmethyl>amine

1.2 Other means of identification

Product number -
Other names (4-fluorophenyl)(phenyl)methanamine

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:55095-26-6 SDS

55095-26-6Relevant articles and documents

Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis

Wang, Hongyu,Man, Yunquan,Wang, Kaiye,Wan, Xiuyan,Tong, Lili,Li, Na,Tang, Bo

, p. 10989 - 10992 (2018/10/08)

An application of H-bonding interactions for directing the α-C-H oxidation of amines to amides and amino-ketones catalyzed by an organic photocatalyst is reported. The high efficiency of this method is demonstrated by the aerobic oxidation of pyrrolidines, diarylamines and benzylamines bearing urea groups with high yields and a wide substrate scope.

DOPAMINE D2 RECEPTOR LIGANDS

-

Page/Page column 115; 117; 125; 126; 129, (2016/07/05)

The present invention relates to novel dopamine D2 receptor ligands. The invention further relates to functionally-biased dopamine D2 receptor ligands and the use of these compounds for treating or preventing central nervous system and systemic disorders associated with dysregulation of dopaminergic activity.

PYRROLOPYRIDINE DERIVATIVE AND USE THEREOF

-

Page/Page column 45, (2008/06/13)

A novel pyrrolopyridine derivative which is a compound represented by the formula ???wherein Ring A represents an optionally substituted pyridine ring; X represents an electron-attracting group; Y represents an optionally substituted divalent C1-6 chain hydrocarbon group; R1 represents an optionally substituted hydrocarbon group; and R2 and R3 each independently represents hydrogen, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, or R2 and R3 may form an optionally substituted ring in cooperation with the adjacent nitrogen atom, or a salt of the compound. The pyrrolopyridine derivative has vanilloid receptor agonist activity and is useful as medicines such as a preventive/therapeutic agent and analgesic for overactive bladder.

A practical synthesis of para di- and mono-substituted benzhydrylamines from benzhydrol precursors

Laurent, Mathieu,Marchand-Brynaert, Jacqueline

, p. 667 - 672 (2007/10/03)

A series of para-substituted benzhydrylamines 6 were obtained by substitution of the corresponding benzhydrol precursors 1 with phenyl carbamate 2 under acidic conditions, followed by basic hydrolysis of the carbamate intermediates 3. One unsymmetrical intermediate 3i has been resolved by preparative chiral chromatography. Subsequent deprotection of the carbamate function led to the recovery of enantiomerically pure (+)- and (-)- 4-chlorobenzhydryl amines.

Substituted benzhydryl lactamimide derivatives

-

, (2008/06/13)

Novel compounds useful as diuretic agents and anticoagulants are represented by the following formula SPC1 Wherein m is a positive whole integer of from 1 to 3; n is a positive whole integer of from 3 to 7; R and R1 may be the same or different

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