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101925-47-7

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101925-47-7 Usage

General Description

H-NVA-NH2 HCL is a chemical compound consisting of a hydrochloride salt form of N-palmitoyl-L-valine amide (H-NVA-NH2), a synthetic amino acid derivative. H-NVA-NH2 HCL has been studied for its potential use as a drug delivery system and for its antimicrobial properties. It is also being investigated for its potential in drug conjugate therapy and liposomal drug delivery systems. H-NVA-NH2 HCL has shown promising results in preclinical studies, and further research is being conducted to explore its therapeutic potential in various healthcare applications.

Check Digit Verification of cas no

The CAS Registry Mumber 101925-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,2 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101925-47:
(8*1)+(7*0)+(6*1)+(5*9)+(4*2)+(3*5)+(2*4)+(1*7)=97
97 % 10 = 7
So 101925-47-7 is a valid CAS Registry Number.

101925-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-Aminopentanamide hydrochloride

1.2 Other means of identification

Product number -
Other names (2S)-2-aminopentanamide,hydrochloride

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:101925-47-7 SDS

101925-47-7Upstream product

101925-47-7Downstream Products

101925-47-7Relevant articles and documents

A convenient synthesis of (S)-2-azidonitriles, (S)-2-aminonitriles and (S)-1,2-diamines

Effenberger,Kremser, Andreas,Stelzer, Uwe

, p. 607 - 618 (2007/10/03)

(S)-2-Azidonitriles (S)-4 are easily accessible from (R)-2-(sulfonyloxy)nitriles (R)-2 by nucleophilic substitution with alkali azides 3 under complete inversion of configuration. The azidonitriles (S)-4 can be converted by catalytic hydrogenation into (S)-2-aminonitriles (S)-8 and by hydrogenation using LiAlH4 into (S)-1,2-diaminoalkanes (S)-9, respectively, both, (S)-8 and (S)-9, isolated as hydrochlorides. Hydrolysis of the aminonitrile hydrochlorides (S)-8·HCl in a saturated solution of HCl in alcohol gives (S)-2-amino carboxamide hydrochlorides (S)-10·HCl with enantiomeric excesses >99% after recrystallization.

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