Welcome to LookChem.com Sign In|Join Free
  • or
Boc-D-Phe-Phe-OBzl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97642-16-5

Post Buying Request

97642-16-5 Suppliers

Recommended suppliers

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

97642-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97642-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,4 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97642-16:
(7*9)+(6*7)+(5*6)+(4*4)+(3*2)+(2*1)+(1*6)=165
165 % 10 = 5
So 97642-16-5 is a valid CAS Registry Number.

97642-16-5Downstream Products

97642-16-5Relevant academic research and scientific papers

METHOD FOR PRODUCING CARBOXYLIC ACID AMIDE COMPOUND, AND CATALYST AND FLOW PRODUCTION SYSTEM

-

Paragraph 0048-0066; 0068; 0070-0079, (2021/09/03)

PROBLEM TO BE SOLVED: To provide a new production method that allows a dehydration condensation reaction between carboxylic acid and amine, and a catalyst. SOLUTION: A method for producing a carboxylic acid amide compound includes the step for causing a r

Mortiamides A-D, Cyclic Heptapeptides from a Novel Mortierella sp. Obtained from Frobisher Bay

Grunwald, Alyssa L.,Berrue, Fabrice,Robertson, Andrew W.,Overy, David P.,Kerr, Russell G.

supporting information, p. 2677 - 2683 (2017/11/06)

Four new cyclic heptapeptides, mortiamides A-D (1-4), were obtained from a novel Mortierella sp. isolate obtained from marine sediment collected from the intertidal zone of Frobisher Bay, Nunavut, Canada. The structures of the compounds were elucidated by NMR spectroscopy and tandem mass spectrometry. The absolute configurations of the amino acids were determined using Marfey's method. Localization of l and d amino acids within each compound was ascertained by retention time comparison of the partial hydrosylate products of each compound to synthesized dipeptide standards using LC-HRMS. Compounds 1-4 did not exhibit any significant antimicrobial or cytotoxic activity.

LYSOBACTIN AMIDES

-

, (2009/08/18)

The invention relates to lysobactin amides and methods for their preparation, as well as their use for manufacturing medicaments for the treatment and/or prophylaxis of diseases, in particular bacterial infectious diseases.

Studies on neurokinin antagonists. 1. The design of novel tripeptides possessing the glutaminyl-D-tryptophylphenylalanine sequence as substance P antagonists

Hagiwara,Miyake,Morimoto,Murai,Fujii,Matsuo

, p. 2015 - 2025 (2007/10/02)

To discover a novel and low molecular weight substance P (SP) antagonist we postulated that the essential binding domain of peptide ligands was only a small portion in the whole structure. On the basis of this assumption, we selected the known octapeptide

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 97642-16-5