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AC-VAL-NHME is a modified form of the amino acid valine, featuring an N-methyl group attached to the amino group. This alteration can influence the amino acid's interactions with other molecules and its biological activity, making it a valuable compound in peptide and protein research for the development of peptides and proteins with tailored structural and functional characteristics.

19701-84-9

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19701-84-9 Usage

Uses

Used in Pharmaceutical Research:
AC-VAL-NHME is used as a research compound for the synthesis of peptides and proteins with specific structural and functional properties. Its unique modification can potentially enhance the stability, solubility, or activity of the resulting biomolecules, contributing to the development of novel therapeutic agents.
Used in Biochemical Studies:
In the field of biochemistry, AC-VAL-NHME is utilized to investigate the role of amino acid modifications in biological processes. By studying the effects of the N-methyl group on the amino acid's interactions and biological activity, researchers can gain insights into the mechanisms underlying protein function and regulation.
Used in Drug Design and Development:
AC-VAL-NHME is employed as a building block in the design and development of new drugs. Its unique properties can be leveraged to create molecules with improved pharmacokinetic and pharmacodynamic profiles, leading to more effective and safer therapeutics.
Used in Peptide Synthesis:
In the synthesis of peptides, AC-VAL-NHME is used as a modified amino acid to introduce specific structural features or functional groups into the peptide sequence. This can result in peptides with enhanced biological activity, selectivity, or stability, which can be applied in various therapeutic or diagnostic applications.
Used in Protein Engineering:
AC-VAL-NHME is utilized in protein engineering to create proteins with altered properties or novel functions. By incorporating the modified amino acid into the protein sequence, researchers can explore the effects of the N-methyl group on protein folding, stability, and interactions with other biomolecules, paving the way for the development of engineered proteins with improved performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19701-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19701-84:
(7*1)+(6*9)+(5*7)+(4*0)+(3*1)+(2*8)+(1*4)=119
119 % 10 = 9
So 19701-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N2O2/c1-5(2)7(8(12)9-4)10-6(3)11/h5,7H,1-4H3,(H,9,12)(H,10,11)/t7-/m0/s1

19701-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-acetamido-N,3-dimethylbutanamide

1.2 Other means of identification

Product number -
Other names N-Acetyl-L-valin-methylamid

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:19701-84-9 SDS

19701-84-9Downstream Products

19701-84-9Relevant articles and documents

Application of C-Terminal 7-Azabicyclo[2.2.1]heptane to Stabilize β-Strand-like Extended Conformation of a Neighboring α-Amino Acid

Zhai, Luhan,Wang, Siyuan,Nara, Masayuki,Takeuchi, Koh,Shimada, Ichio,Otani, Yuko,Ohwada, Tomohiko

, p. 13063 - 13079 (2018/10/25)

β-Strands are formed by extended linear peptide chains that are usually paired to form β-sheet structure through interstrand hydrogen bonding. Linking a structured organic molecule with α-amino acid(s) can enforce or stabilize β-strand-like extended struc

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

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