Welcome to LookChem.com Sign In|Join Free
  • or
threo-2-fluoro-1,2-diphenylethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71057-08-4

Post Buying Request

71057-08-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

71057-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71057-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,5 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71057-08:
(7*7)+(6*1)+(5*0)+(4*5)+(3*7)+(2*0)+(1*8)=104
104 % 10 = 4
So 71057-08-4 is a valid CAS Registry Number.

71057-08-4Downstream Products

71057-08-4Relevant academic research and scientific papers

Hydrogen Bonding Phase-Transfer Catalysis with Potassium Fluoride: Enantioselective Synthesis of β-Fluoroamines

Pupo, Gabriele,Vicini, Anna Chiara,Ascough, David M. H.,Ibba, Francesco,Christensen, Kirsten E.,Thompson, Amber L.,Brown, John M.,Paton, Robert S.,Gouverneur, Véronique

supporting information, p. 2878 - 2883 (2019/02/14)

Potassium fluoride (KF) is an ideal reagent for fluorination because it is safe, easy to handle and low-cost. However, poor solubility in organic solvents coupled with limited strategies to control its reactivity has discouraged its use for asymmetric C-F

Chiral monofluorobenzyl carbanions: Synthesis of enantiopure β-fluorinated β-phenylethylamines

Garcia Ruano, Jose L.,Parra, Alejandro,Alonso, Ines,Fustero, Santos,Del Pozo, Carlos,Arroyo, Yolanda,Sanz-Tejedor, Ascension

experimental part, p. 6142 - 6147 (2011/06/24)

The preparation of a stabilized monofluorobenzyl carbanion by means of a remote homochiral sulfinyl group and its completely stereoselective reactions with N-p-tolylsulfinylimines are described. The use of these reactions followed by the simultaneous remo

SELECTIVE REDUCTION OF β-FLUOROAZIDES TO β-FLUOROAMINES

Hamman, S.,Beguin, C.G.

, p. 191 - 196 (2007/10/02)

Three methods were tested to reduce chemoselectively β-fluoroazides into β-fluoroamines : catalytic hydrogenation, catalytic transfer hydrogenation, and reduction with triphenyl phosphine.The last was the best.

Ring Opening of Aziridines by Different Fluorinating Reagents: Three Synthetic Routes to α,β-Fluoro Amines with Different Stereochemical Pathways

Alvernhe, Gerald M.,Ennakoua, Christine M.,Lacombe, Sylvie M.,Laurent, Andre J.

, p. 4938 - 4948 (2007/10/02)

The syntheses of α,β-fluoro amines from the reaction of secondary aziridines with either Olah's reagent (HF, pyridine) or anhydrous hydrogen fluoride and of N-activated aziridines with partially neutralized Olah's reagent (NR3-nHF) are reported.The stereo

Preparation of Fluoro Amines by the Reaction of Aziridines with Hydrogen Fluoride in Pyridine Solution

Wade, Tamsir N.

, p. 5328 - 5333 (2007/10/02)

Hydrogen fluoride combines regiospecifically with aziridines (1) to give 2-fluoro amines (6) in good yields.Fluorine attack is in all cases completely directed to the most substituted ring carbon or to the benzylic carbon.The results, for benzylic aziridi

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 71057-08-4