Welcome to LookChem.com Sign In|Join Free
  • or
ethyl (3R)-2-(3-methylcyclohexylidene)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221157-79-5

Post Buying Request

221157-79-5 Suppliers

Recommended suppliers

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

221157-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221157-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,5 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 221157-79:
(8*2)+(7*2)+(6*1)+(5*1)+(4*5)+(3*7)+(2*7)+(1*9)=105
105 % 10 = 5
So 221157-79-5 is a valid CAS Registry Number.

221157-79-5Relevant academic research and scientific papers

Esterase-mediated synthesis of optically active GABA analogues containing a stereogenic all-carbon quaternary carbon atom

Felluga, Fulvia,Ghelfi, Franco,Pitacco, Giuliana,Roncaglia, Fabrizio,Valentin, Ennio,Venneri, Cesare Daniele

experimental part, p. 2183 - 2191 (2010/10/03)

Esterase from Horse Liver (HLAP) was able to hydrolyze a series of linear and cyclic β,β-dialkyl-γ-nitroesters, in spite of the well-known reluctance of hydrolytic enzymes to recognize and transform hindered substrates, such as those possessing a stereoge

A Novel and Highly Stereoselective Approach to Aza-Spirocycles. A Short Total Synthesis of 2-epi-(±)-Perhydrohistrionicotoxin and an Unprecedented Decarboxylation of 2-Pyrones

McLaughlin, Michael J.,Hsung, Richard P.,Cole, Kevin P.,Hahn, Juliet M.,Wang, Jiashi

, p. 2017 - 2020 (2007/10/03)

(Matrix Presented) A novel and highly stereoselective synthesis of aza-spirocycles is described. An application of this methodology is illustrated as a short and concise total synthesis of 2-epi-(±)-perhydrohistrionicotoxin with high diastereomeric contro

Identification of novel ligands for the Gabapentin binding site on the α2δ subunit of a calcium channel and their evaluation as anticonvulsant agents

Bryans, Justin S.,Davies, Natasha,Gee, Nicolas S.,Dissanayake, Visaka U. K.,Ratcliffe, Giles S.,Horwell, David C.,Kneen, Clare O.,Morrell, Andrew I.,Oles, Ryszard J.,O'Toole, John C.,Perkins, Gemma M.,Singh, Lakhbir,Suman-Chauhan, Nirmala,O'Neill, Jacqueline A.

, p. 1838 - 1845 (2007/10/03)

As part of a program to investigate the structure-activity relationships of Gabapentin (Neurontin), a number of alkylated analogues were synthesized and evaluated in vitro for binding to the Gabapentin binding site located on the α2δ subunit of

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 221157-79-5