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Z-(L)NMeNva, also known as Z-N-methyl-L-norvaline, is a synthetic, non-natural amino acid derivative. It is characterized by the presence of a Z-group (benzyloxycarbonyl) protecting group and an N-methyl group attached to the side chain of L-norvaline, which is a naturally occurring amino acid. Z-(L)NMeNva is often used in peptide synthesis and medicinal chemistry due to its unique properties, such as increased hydrophobicity and potential for enhanced bioactivity. The Z-group serves as a temporary protecting group that can be removed under specific conditions, allowing for the controlled assembly of peptide sequences. Z-(L)NMeNva's role in these applications highlights its importance in the development of new drugs and therapeutics.

19635-90-6

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19635-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19635-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,3 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19635-90:
(7*1)+(6*9)+(5*6)+(4*3)+(3*5)+(2*9)+(1*0)=136
136 % 10 = 6
So 19635-90-6 is a valid CAS Registry Number.

19635-90-6SDS

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 Z-(L)NMeNva

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-methyl-L-norvalin

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:19635-90-6 SDS

19635-90-6Relevant academic research and scientific papers

Destruxin analogues: Depsi peptidic bond replacement by amide bond

Cavelier,Jacquier,Mercadier,Verducci

, p. 6173 - 6186 (2007/10/03)

In order to determine the importance of the depsi bond present in natural destruxins, we have investigated the replacement of this ester bond by an amide bond, leading to a new family of analogues. Synthesis of six specific members of this new class of compounds is reported. Since none of these cyclopeptides showed any biological activity, we undoubtedly proved that the depside group is a requisite for insecticide effect.

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