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2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpr...

2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid

CAS: 80542-76-3

Molecular Formula: C22H21N3O5S

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2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpr... - Names and Identifiers

Name 2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid
Synonyms 2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpr...
2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid
2-[(2-AMINO-THIAZOL-4-YL)-CARBOXY-METHYLENEAMINOXY]-2-METHYL-PROPIONIC ACID
2-((2-amino-Thiazol-4-yl)-carboxy-methyleneaminooxyl)-2-methyl-propionicacid
2-[(2-AMINO-THIAZOL-4-YL)-CARBOXY-METHYLENEAMINOOXY]-2-METHYL-PROPIONIC ACID
2-[[(2-amino-4-thiazolyl)-carboxymethylidene]amino]oxy-2-methylpropanoic acid
4-Thiazoleacetic acid, 2-amino-α-[[2-(diphenylmethoxy)-1,1-dimethyl-2-oxoethoxy]imino]-, (Z)- (9CI)
2-[(2-amino-thiazol-4-yl)-carboxy-methyleneaminoxy]-2-methyl-propionic acid (intermediate of aztreonam)
2-[(2-Amino-Thiazol-4-Yl)-Carboxy-Methyleneaminooxy]-2-Methyl-Propionic Acid (The Intermediate Of Aztreonam)
CAS 80542-76-3
InChI InChI=1/C9H11N3O5S/c1-9(2,7(15)16)17-12-5(6(13)14)4-3-18-8(10)11-4/h3H,1-2H3,(H2,10,11)(H,13,14)(H,15,16)

2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpr... - Physico-chemical Properties

Molecular FormulaC22H21N3O5S
Molar Mass439.48
Density1.33±0.1 g/cm3(Predicted)
Boling Point627.2±65.0 °C(Predicted)
pKa2.55±0.10(Predicted)
Refractive Index1.658

2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpr... - Introduction

2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid, also known as ACMA(2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid).

Nature:
ACMA is a white to pale yellow crystalline solid with a chemical formula C10H12N4O5S and a relative molecular mass of 292.299g/mol. It has high solubility in water.

Use:
ACMA has some important applications in medicine and chemistry. It is mainly used as an intermediate and plays a key role in drug research and synthesis. ACMA can also be used for nucleophilic substitution reactions, coupling reactions and removal of protecting groups in organic synthesis. In addition, it can also be used as a precursor of ultrasound contrast agents and anti-tumor drugs.

Preparation Method:
There are various methods for preparing ACMA. A common synthetic method is the reaction of 2-aminothiazole-4-carbaldehyde with a hydroxylamine salt to give 2-[(2-Aminothiazol-4-yl)carboxymethyleneaminooxy]-2-methylpropionic acid.

Safety Information:
The safety of ACMA varies depending on the specific environment and use. When handling and storing ACMA, appropriate protective measures should be taken, such as wearing protective gloves and glasses, and maintaining good ventilation conditions. When using ACMA, the relevant safety procedures and personal protective measures should be strictly observed. If you ingest or come into contact with ACMA, you should seek medical help immediately.
Last Update:2024-04-09 15:18:00
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