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Formamide, N-[(3-fluorophenyl)methyl](9CI) is a chemical compound with the molecular formula C8H8FNO. It belongs to the formamide group and is an organic compound that is commonly used as a solvent and reagent in various chemical reactions. This specific formamide contains a fluorophenyl group, which makes it suitable for pharmaceutical and agrochemical research. It may also have potential applications in the development of new materials and compounds. However, due to its potential health and environmental hazards, it should be handled with caution.

180207-86-7

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180207-86-7 Usage

Uses

Used in Pharmaceutical Research:
Formamide, N-[(3-fluorophenyl)methyl](9CI) is used as a reagent in pharmaceutical research for the synthesis of various compounds. Its fluorophenyl group provides unique properties that can be utilized in the development of new drugs and pharmaceuticals.
Used in Agrochemical Research:
In agrochemical research, Formamide, N-[(3-fluorophenyl)methyl](9CI) is used as a reagent for the synthesis of agrochemicals. Its unique properties can contribute to the development of new pesticides, herbicides, and other agrochemicals.
Used in Material Science:
Formamide, N-[(3-fluorophenyl)methyl](9CI) has potential applications in the development of new materials and compounds in material science. Its unique structure and properties can be utilized to create innovative materials with specific characteristics.
Used in Chemical Reactions:
As a solvent and reagent, Formamide, N-[(3-fluorophenyl)methyl](9CI) is used in various chemical reactions to facilitate the synthesis of different compounds. Its versatility makes it a valuable component in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 180207-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,2,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 180207-86:
(8*1)+(7*8)+(6*0)+(5*2)+(4*0)+(3*7)+(2*8)+(1*6)=117
117 % 10 = 7
So 180207-86-7 is a valid CAS Registry Number.

180207-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3-fluorophenyl)methyl]formamide

1.2 Other means of identification

Product number -
Other names W3915

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:180207-86-7 SDS

180207-86-7Downstream Products

180207-86-7Relevant academic research and scientific papers

ZIF-67 Derived Co/NC Nanoparticles Enable Catalytic Leuckart-type Reductive Amination of Bio-based Carbonyls to N-Formyl Compounds

Li, Chuanhui,Meng, Ye,Yang, Song,Li, Hu

, p. 5166 - 5177 (2021/10/25)

It is of great significance to develop non-precious metal catalysts with excellent catalytic activity, stability, and acid resistance for biomass valorization. Herein, catalytic amination of biomass carbonyl compounds was achieved via a Leuckart-type reaction over Co nanoparticles (NPs) embedded N-doped carbon catalyst, which was prepared by thermolysis of ZIF-67 precursor at different temperatures in the N2 atmosphere. The Co/NC-800 catalyst exhibited excellent catalytic activity and recyclability in furfural reductive amination to mono-substituted formamide, which was attributed to the synergistic catalytic action of Co NPs and nitrogen base sites of the catalyst. The reductive amination mechanisms were elucidated by theoretical calculations, and showed that the initial formation of C?N bond was derived from the condensation of furfural and formamide, followed by dehydration to form C=N double bond, which was then reduced by hydrogen species Co?H? and NH+. The developed catalytic system was applicable to different carbonyls for the synthesis of corresponding N-formyl compounds with up to 99 % yield.

Leuckart-Wallach Route Toward Isocyanides and Some Applications

Neochoritis, Constantinos G.,Zarganes-Tzitzikas, Tryfon,Stotani, Silvia,D?mling, Adrian,Herdtweck, Eberhardt,Khoury, Kareem,D?mling, Alexander

supporting information, p. 493 - 499 (2015/09/22)

Isocyanide-based multicomponent reactions (IMCR) are among the most important chemical reactions to efficiently generate molecular diversity and have found widespread use in industry and academia. Generally, isocyanides are synthesized in 1-2 steps starting from primary amines. Here, we provide experimental detail on an alternative approach toward formamides and, thus, isocyanides via the Leuckart-Wallach reaction in an improved variation. The resulting >50 synthesized and characterized formamides are useful starting materials for IMCR, as well as other chemistries. The advantage of using the Leuckart-Wallach pathway to formamides and isocyanides is the lower price, on average, of the starting materials, as well as their differential and complementary structural diversity, as compared to the primary amine pathway.

3-Phenyl-substituted imidazo[1,5-a]quinoxalin-4-ones and imidazo[1,5- a]quinoxaline ureas that have high affinity at the GABA(A)/benzodiazepine receptor complex

Jacobsen, E. Jon,Stelzer, Lindsay S.,Belonga, Kenneth L.,Carter, Donald B.,Im, Wha Bin,Sethy, Vimala H.,Tang, Andrew H.,Von Voigtlander, Philip F.,Petke, James D.

, p. 3820 - 3836 (2007/10/03)

A series of imidazo[1,5-a]quinoxalin-4-ones and imidazo[1,5- a]quinoxaline ureas containing substituted phenyl groups at the 3-position was developed. Compounds within the imidazo-[1,5-a]quinoxaline urea series had high affinity for the GABA(A)/benzodiaze

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