Welcome to LookChem.com Sign In|Join Free
  • or
L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester is a complex organic compound derived from the essential amino acid L-Valine. It features a cyanoacetyl group, a dimethylbutyl group, and a methyl ester group, which together confer unique chemical properties and potential applications in various fields. The presence of these functional groups suggests that L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester may have roles in pharmaceutical development, agrochemicals, or as a building block in organic synthesis.

1162665-53-3

Post Buying Request

1162665-53-3 Suppliers

Recommended suppliers

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

1162665-53-3 Usage

Uses

Used in Pharmaceutical Development:
L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester is used as a chemical intermediate for the synthesis of pharmaceutical drugs. Its unique structure allows for the development of new drug candidates that may have therapeutic effects in treating various diseases.
Used in Agrochemicals:
In the agrochemical industry, L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester is used as a building block for the creation of new agrochemicals. Its properties may contribute to the development of more effective and environmentally friendly pesticides or herbicides.
Used in Organic Synthesis:
L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester is used as a versatile building block in organic synthesis. Its functional groups can be utilized in the preparation of a wide range of organic compounds, including specialty chemicals, fragrances, and other commercially important products.
Used in Research and Development:
In the field of research and development, L-Valine, N-(2-cyanoacetyl)-N-(3,3-dimethylbutyl)-3-methyl-, methyl ester serves as a valuable compound for studying the effects of its unique structure on various chemical and biological processes. This can lead to a better understanding of its potential applications and the discovery of new uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1162665-53-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,2,6,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1162665-53:
(9*1)+(8*1)+(7*6)+(6*2)+(5*6)+(4*6)+(3*5)+(2*5)+(1*3)=153
153 % 10 = 3
So 1162665-53-3 is a valid CAS Registry Number.

1162665-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[(2-cyanoacetyl)-(3,3-dimethylbutyl)amino]-3,3-dimethylbutanoate

1.2 Other means of identification

Product number -
Other names VAL009

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:1162665-53-3 SDS

1162665-53-3Downstream Products

1162665-53-3Relevant academic research and scientific papers

Discovery of benzophosphadiazine drug candidate IDX375: A novel hepatitis C allosteric NS5B RdRp inhibitor

Paparin, Jean-Laurent,Amador, Agnès,Badaroux, Eric,Bot, Stéphanie,Caillet, Catherine,Convard, Thierry,Da Costa, Daniel,Dukhan, David,Griffe, Ludovic,Griffon, Jean-Fran?ois,LaColla, Massimiliano,Leroy, Frédéric,Liuzzi, Michel,Giulia Loi, Anna,McCarville, Joe,Mascia, Valeria,Milhau, Julien,Onidi, Loredana,Pierra, Claire,Rahali, Rachid,Rosinosky, Elodie,Sais, Efisio,Seifer, Maria,Surleraux, Dominique,Standring, David,Dousson, Cyril B.

, p. 2634 - 2640 (2017)

Hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase (RdRp) plays a central role in virus replication. NS5B has no functional equivalent in mammalian cells, and as a consequence is an attractive target for selective inhibition. This paper describes the discovery of a novel family of HCV NS5B non-nucleoside inhibitors inspired by the bioisosterism between sulfonamide and phosphonamide. Systematic structural optimization in this new series led to the identification of IDX375, a potent non-nucleoside inhibitor that is selective for genotypes 1a and 1b. The structure and binding domain of IDX375 were confirmed by X-ray co-crystalisation study.

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 1162665-53-3