Welcome to LookChem.com Sign In|Join Free
  • or
tert-butyl 2-[fluoro(phenyl)methyl]acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1571082-52-4

Post Buying Request

1571082-52-4 Suppliers

Recommended suppliers

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

1571082-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1571082-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,0,8 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1571082-52:
(9*1)+(8*5)+(7*7)+(6*1)+(5*0)+(4*8)+(3*2)+(2*5)+(1*2)=154
154 % 10 = 4
So 1571082-52-4 is a valid CAS Registry Number.

1571082-52-4Relevant academic research and scientific papers

Enantioselective Lewis base catalyzed phosphonyldifluoromethylation of allylic fluorides using a: C -silyl latent pronucleophile

Zi, You,Lange, Markus,Vilotijevic, Ivan

, p. 5689 - 5692 (2020)

The first enantioselective phosphonyldifluoromethylation is enabled by the use of diethyl (difluoro(trimethylsilyl)-methyl)phosphonate reagent as a latent pronucleophile in the Lewis base catalyzed substitution of allylic fluorides. The reaction proceeds

Synthesis of Morita–Baylis–Hillman-fluorides using 1,1,2,2-tetrafluoroethyl-N,N-dimethylamine

Sumii, Yuji,Nagasaka, Takato,Matsuno, Ayaka,Hayashi, Hidetoshi,Mimura, Hideyuki,Kagawa, Takumi,Shibata, Norio

, (2021/08/18)

Morita–Baylis–Hillman (MBH)-fluorides are valuable platforms for asymmetric allylic substitution reactions. However, the preparation of MBH-fluorides requires the use of an explosive fluorinating reagent, namely (diethylamino)sulfur trifluoride (DAST). Th

Enantioselective Trichloromethylation of MBH-Fluorides with Chloroform Based on Silicon-assisted C-F Activation and Carbanion Exchange Induced by a Ruppert-Prakash Reagent

Nishimine, Takayuki,Taira, Hiromi,Tokunaga, Etsuko,Shiro, Motoo,Shibata, Norio

supporting information, p. 359 - 363 (2016/01/25)

Enantioselective trichloromethylation of Morita-Baylis-Hillman (MBH)-type allylic fluorides with chloroform (HCCl3) under organocatalysis was achieved with high to excellent enantioselectivities. Silicon-assisted C-F bond activation by a Rupper

Kinetic resolution of allyl fluorides by enantioselective allylic trifluoromethylation based on silicon-assisted c-F bond cleavage

Nishimine, Takayuki,Fukushi, Kazunobu,Shibata, Naoyuki,Taira, Hiromi,Tokunaga, Etsuko,Yamano, Akihito,Shiro, Motoo,Shibata, Norio

supporting information, p. 517 - 520 (2014/01/23)

Two birds, one stone! The first kinetic resolution of allyl fluorides was achieved by the development of an organocatalyzed enantioselective allylic trifluoromethylation. Two kinds of chiral fluorinated compounds, which incorporate C-F and C-CF3 units, respectively, can thus be accessed by a single transformation.

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 1571082-52-4