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161754-60-5

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161754-60-5 Usage

General Description

"(S)-N-(2,2-DIFLUOROETHYLIDENE)-1-PHENYLETHYLAMINE" is a chemical compound with the molecular formula C10H12F2N. It is a chiral amine with a difluoroethylidene substituent attached to a phenylethylamine backbone. (S)-N-(2,2-DIFLUOROETHYLIDENE)-1-PHENYLETHYLAMINE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure and properties make it suitable for use in various chemical reactions and transformations, making it a valuable building block in organic synthesis. Its potential applications include the development of new drugs, pesticides, and other important compounds in the fields of medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 161754-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,7,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161754-60:
(8*1)+(7*6)+(6*1)+(5*7)+(4*5)+(3*4)+(2*6)+(1*0)=135
135 % 10 = 5
So 161754-60-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11F2N/c1-8(13-7-10(11)12)9-5-3-2-4-6-9/h2-8,10H,1H3/b13-7+/t8-/m0/s1

161754-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoro-N-[(1S)-1-phenylethyl]ethanimine

1.2 Other means of identification

Product number -
Other names D2524

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:161754-60-5 SDS

161754-60-5Downstream Products

161754-60-5Relevant articles and documents

Highly diastereo- and enantioselective vinylogous Mannich reactions of fluorinated aldimines with siloxyfurans

Zhao, Qian-Yi,Yuan, Zhi-Liang,Shia, Min

supporting information; experimental part, p. 637 - 643 (2011/04/25)

A highly regio- and enantioselective asymmetric vinylogous Mannich reaction of readily available fluorinated aldimines bearing a chiral auxiliary [(S)-1-phenylethyl group] with siloxyfurans to afford chiral fluorine-containing γ-butenolide or γ-lactone derivatives has been developed in the presence of silver acetate (10 mol%) and axially chiral phosphine-oxazoline ligand L1 (11 mol%). In most cases, the corresponding fluorinated adducts were obtained in high yields, good to excellent enantiomeric excesses and up to > 20:1 dr.

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