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2-AMINO-N-(BENZYLOXY)-ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16975-23-8

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16975-23-8 Usage

Chemical compound

2-AMINO-N-(BENZYLOXY)-ACETAMIDE

Usage

Used in the synthesis of pharmaceutical drugs and may have potential medicinal applications

Usage in research

Used in organic chemistry research as a building block for the synthesis of various organic molecules

Physical appearance

White crystalline solid

Solubility

Soluble in organic solvents

Melting point

Around 170-172°C

Check Digit Verification of cas no

The CAS Registry Mumber 16975-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16975-23:
(7*1)+(6*6)+(5*9)+(4*7)+(3*5)+(2*2)+(1*3)=138
138 % 10 = 8
So 16975-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O2/c10-6-9(12)11-13-7-8-4-2-1-3-5-8/h1-5H,6-7,10H2,(H,11,12)

16975-23-8SDS

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 2-amino-N-phenylmethoxyacetamide

1.2 Other means of identification

Product number -
Other names 2-Amino-N-(benzyloxy)-acetamide

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:16975-23-8 SDS

16975-23-8Relevant academic research and scientific papers

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE

-

, (2017/09/28)

The invention relates to a compound of Formula (I), or pharmaceutically acceptable enantiomers, or salts thereof. The present invention also relates to the use of compounds of Formula (I) as selective inhibitors of indoleamine 2,3-dioxygenase. The inventi

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Mai, Anh Hung,Pawar, Sonalika,De Borggraeve, Wim M.

supporting information, p. 4664 - 4666 (2014/12/10)

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.

CARBAMATE COMPOUNDS AND OF MAKING AND USING SAME

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Paragraph 00182, (2013/10/08)

Provided herein are carbamate compounds which may be useful in the treatment of, for example, pain, solid tumors and/or obesity.

Quantum chemistry-based interpretations on the lowest triplet state of luminescent lanthanides complexes. Part 1. Relation between the triplet state energy of hydroxamate complexes and their luminescence properties

Gutierrez, Fabien,Tedeschi, Christine,Maron, Laurent,Daudey, Jean-Pierre,Poteau, Romuald,Azema, Joelle,Tisnes, Pierre,Picard, Claude

, p. 1334 - 1347 (2007/10/03)

In this paper, we evaluate the potential use of theoretical calculations to obtain an energy scale of the lowest ligand-centred triplet excited state in luminescent terbium(m) complexes. In these complexes, non-radiative deactivation of the terbium emitti

N-Hydroxyamide-containing Heterocycles. New Effective Additives for Peptide Synthesis by the Dicyclohexylcarbodiimide Method

Katoh, Akira,Ohkanda, Junko,Itoh, Yoshifumi,Mitsuhashi, Keiryo

, p. 2009 - 2012 (2007/10/02)

N-Hydroxyamide-containing heterocycles, 1-hydroxy-4,6-dimethyl-2(1H)-pyrimidinone and -5,6-dimethyl-2(1H)-pyrazinone, are prepared.Judging from the result of model dipeptide (Z-Ala-Phe-OMe) formation, these compounds are found to be new effective additive

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