Welcome to LookChem.com Sign In|Join Free
  • or
3-(4-Aminonaphthalen-1-yl)-N-BOC-L-alanine, also known as Boc-L-A-A-Naph-1-NH2, is a complex amino acid compound that combines the properties of naphthalene and alanine. It features an amine group attached to the first position of the naphthalene molecule, which contributes to its unique characteristics. The N-t-butyloxycarbonyl (Boc) group in the compound serves as a protective functional group for amines during organic synthesis. This chemical is primarily used in scientific research and the pharmaceutical industry, where it plays a crucial role in the development and testing of drugs.

436864-62-9

Post Buying Request

436864-62-9 Suppliers

Recommended suppliers

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

436864-62-9 Usage

Uses

Used in Scientific Research:
3-(4-Aminonaphthalen-1-yl)-N-BOC-L-alanine is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure and the presence of the Boc group make it an interesting subject for exploration in the realm of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(4-Aminonaphthalen-1-yl)-N-BOC-L-alanine is used as a building block in the synthesis of complex molecules and drug candidates. Its incorporation into drug molecules can potentially enhance their therapeutic properties, such as improving their stability, solubility, or bioavailability.
Used in Drug Development:
3-(4-Aminonaphthalen-1-yl)-N-BOC-L-alanine is used as a key intermediate in the development of new drugs. Its presence in a drug molecule can contribute to the overall efficacy and safety profile of the final product, making it a valuable component in the drug discovery process.
Used in Laboratory Research:
3-(4-Aminonaphthalen-1-yl)-N-BOC-L-alanine is used as a reagent in laboratory experiments, where it can be employed to study the interactions between different chemical entities or to test the effects of modifications to its structure on the properties of the resulting compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 436864-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,8,6 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 436864-62:
(8*4)+(7*3)+(6*6)+(5*8)+(4*6)+(3*4)+(2*6)+(1*2)=179
179 % 10 = 9
So 436864-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H22N2O4/c1-18(2,3)24-17(23)20-15(16(21)22)10-11-8-9-14(19)13-7-5-4-6-12(11)13/h4-9,15H,10,19H2,1-3H3,(H,20,23)(H,21,22)/t15-/m0/s1

436864-62-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-(4-aminonaphthalen-1-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:436864-62-9 SDS

436864-62-9Relevant academic research and scientific papers

Selective protein tyrosine phosphatatase inhibitors

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts thereof, are selective protein tyrosine kinase-B (PTP1B) inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of disorders using the compounds are disclosed.

Discovery of a potent, selective protein tyrosine phosphatase 1B inhibitor using a linked-fragment strategy

Szczepankiewicz, Bruce G.,Liu, Gang,Hajduk, Philip J.,Abad-Zapatero, Cele,Pei, Zhonghua,Xin, Zhili,Lubben, Thomas H.,Trevillyan, James M.,Stashko, Michael A.,Ballaron, Stephen J.,Liang, Heng,Huang, Flora,Hutchins, Charles W.,Fesik, Stephen W.,Jirousek, Michael R.

, p. 4087 - 4096 (2007/10/03)

Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that downregulates the insulin receptor. Inhibition of PTP1B is expected to improve insulin action, and the design of small molecule PTP1B inhibitors to treat type II diabetes has received considerable attention. In this work, NMR-based screening identified a nonselective competitive inhibitor of PTP1B. A second site ligand was also identified by NMR-based screening and then linked to the catalytic site ligand by rational design. X-ray data confirmed that the inhibitor bound with the catalytic site in the native, "open" conformation. The final compound displayed excellent potency and good selectivity over many other phosphatases. The modular approach to drug design described in this work should be applicable for the design of potent and selective inhibitors of other therapeutically relevant protein tyrosine phosphatases.

Selective protein tyrosine phosphatatase inhibitors

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts thereof, are selective protein tyrosine kinase-B (PTP1B) inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of disorders using the compounds are disclosed.

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 436864-62-9