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60839-94-3

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60839-94-3 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 55, p. 4757, 1990 DOI: 10.1021/jo00302a052

Check Digit Verification of cas no

The CAS Registry Mumber 60839-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,3 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60839-94:
(7*6)+(6*0)+(5*8)+(4*3)+(3*9)+(2*9)+(1*4)=143
143 % 10 = 3
So 60839-94-3 is a valid CAS Registry Number.

60839-94-3SDS

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 fluoromethylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names fluoromethyl phenyl sulphide

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:60839-94-3 SDS

60839-94-3Relevant articles and documents

Fluoromethylated derivatives of carnitine biosynthesis intermediates- synthesis and applications

Rydzik, Anna M.,Leung, Ivanhoe K. H.,Thalhammer, Armin,Kochan, Grazyna T.,Claridge, Timothy D. W.,Schofield, Christopher J.

, p. 1175 - 1177 (2014)

A convenient method for the synthesis of fluoromethylated carnitine biosynthesis intermediates, i.e. fluorinated derivatives of γ- butyrobetaine and trimethyllysine, is described. The fluoromethylated probes were useful in both in vitro and cell based ass

[18F]Fluoromethyl iodide ([18F]FCH2I): Preparation and reactions with phenol, thiophenol, amide and amine functional groups

Zhang, Ming-Rong,Ogawa, Masanao,Furutsuka, Kenji,Yoshida, Yuichiro,Suzuki, Kazutoshi

, p. 1879 - 1886 (2004)

In this study, we report the synthesis and reactivity of [ 18F]fluoromethyl iodide ([18F]FCH2I) with various nucleophilic substrates and the stabilities of [18F] fluoromethylated compounds. [18F]FCHs

Novel process for synthesizing 2 -fluorocyclopropylamine with high selectivity and asymmetric synthesis

-

, (2021/10/13)

A novel highly selective asymmetric synthesis process of 2 -fluorocyclopropylamine (Structural I). The method provided by the invention uses 1 - fluorine -1 - benzene (propylene) sulfonyl methane and chiral epichlorohydrin to construct chiral cyclopropane under basic conditions, and a new synthetic route not only achieves a special cis-trans selectivity, but also has a highly specific stereoselectivity. The synthesis route is efficient, the reaction condition is mild, the method is suitable for large industrial production in a green environment, 2 -fluorocyclopropylamine production cost is greatly reduced.

COMPOUNDS FOR THE TREATMENT OF KINASE-DEPENDENT DISORDERS

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Paragraph 000353, (2020/12/29)

Disclosed herein are compounds of Formula (I) which inhibit, regulate and/or modulate tyrosine kinase receptors, particularly Axl and Mer signal transduction pathways related to the changes in cellular activities, compositions containing the compounds, methods of using the compounds to treat kinase-dependent diseases and conditions, and methods for making the compounds.

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