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19701-84-9

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19701-84-9 Usage

General Description

AC-VAL-NHME is a chemical compound that can be used in peptide and protein research. It is a modified form of the amino acid valine, with an N-methyl group attached to the amino group. This modification can alter the properties of the amino acid, potentially affecting its interactions with other molecules and its biological activity. AC-VAL-NHME may be utilized in the synthesis of peptides and proteins with specific structural and functional properties, and its study may contribute to a better understanding of the role of amino acid modifications in biological processes.

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

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