Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-(2-{Butyl-[2-(3-hydroxy-phenyl)-acetyl]-amino}-octanoylamino)-3-(4-fluoro-3-nitro-phenyl)-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

604004-13-9

Post Buying Request

604004-13-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2-(2-{Butyl-[2-(3-hydroxy-phenyl)-acetyl]-amino}-octanoylamino)-3-(4-fluoro-3-nitro-phenyl)-propionic acid

    Cas No: 604004-13-9

  • Need to discuss

  • No requirement

  • Adequate

  • Afine Chemicals Limited
  • Contact Supplier

604004-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 604004-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,4,0,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 604004-13:
(8*6)+(7*0)+(6*4)+(5*0)+(4*0)+(3*4)+(2*1)+(1*3)=89
89 % 10 = 9
So 604004-13-9 is a valid CAS Registry Number.

604004-13-9Downstream Products

604004-13-9Relevant articles and documents

Rapid and diverse route to natural product-like biaryl ether containing macrocycles

Cristau, Pierre,Vors, Jean-Pierre,Zhu, Jieping

, p. 7859 - 7870 (2007/10/03)

A two-step sequence involving an Ugi four-component reaction and an intramolecular nucleophilic aromatic substitution (SNAr) has been developed for the rapid access to biaryl-ether containing macrocycles. In the course of this study, we documented that ammonium chloride can promote the Ugi-4CR in non-polar aprotic solvent (toluene) without the interference of an alternative Passerini reaction. Solid phase synthesis of macrocycles by this two-step sequence was also developed using polymer (Wang resin) supported α-(4′-fluoro-3′-nitro)phenethyl isocyanoacetate as one of the inputs.

Solid-phase synthesis of natural product-like macrocycles by a sequence of Ugi-4CR and SNAr-based cycloetherification

Cristau, Pierre,Vors, Jean-Pierre,Zhu, Jieping

, p. 5575 - 5578 (2007/10/03)

An on-resin Ugi four-component reaction followed by an intramolecular nucleophilic aromatic substitution (SNAr) has been developed for the rapid access to biaryl-ether containing macrocycles.

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

What can I do for you?
Get Best Price

Get Best Price for 604004-13-9