CAS 22483-09-6

Aminoacetaldehyde dimethyl acetal

Description:

Aminoacetaldehyde dimethyl acetal, with the CAS number 22483-09-6, is an organic compound characterized by its acetal functional group, which is formed from the reaction of an aldehyde with alcohols. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. It is soluble in organic solvents and exhibits moderate stability under standard conditions. The presence of the amino group suggests potential reactivity in various chemical reactions, including nucleophilic substitutions and condensation reactions. Aminoacetaldehyde dimethyl acetal is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, owing to its ability to participate in further chemical transformations. Additionally, it may have applications in the production of specialty chemicals and as a building block in organic synthesis. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

Formula: C₄H₁₁NO₂

InChI: InChI=1/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3/p+1

InChI key: InChIKey=QKWWDTYDYOFRJL-UHFFFAOYSA-N

SMILES: C(CN)(OC)OC

Synonyms:

• 1-Amino-2,2-dimethoxyethane
• 1-Amino-2,2-dimethyloxyethane
• 2,2-Dimethoxyethan-1-amine
• 2,2-Dimethoxyethanamine
• 2,2-Dimethoxyethanaminium
• 2,2-Dimethoxyethylamin
• 2,2-Dimethoxyethylamine
• 2,2-Dimethyethanamine
• 2,2-Dimetoxietilamina
• 2-Aminoacetaldehyde Dimethyl Acetal
• Acetaldehyde, amino-, dimethyl acetal
• Aminoacetal dehyde Dimethyl Acetal
• Aminoacetaldehyde dimethylacetal
• DEA
• Ethanamine, 2,2-dimethoxy-
• Ethylamine, 2,2-dimethoxy-
• Glycinal dimethyl acetal
• N-(2,2-Dimethoxyethyl)amine
• Nsc 73701
• DIMETHYLAMINOACETAL
• AMINOACETOLDEHYDE DIMETHYL ACETOL
• 2-Methoxy-N-[2-methoxyethyl]-1-ethaneamine
• 2-Aminoacetaldehyde dimethylacetal 98%
• 2,2-DIMETHYLETHANAMINE
• Aminoacetaldehyde dimethyl acetal ,98%
• β,β-diethoxy-N,N-dimethylethylamine
• 2-AMINOACETALDEHYDE DIMETHYLACETAL
• 2,2-dimethoxy-ethanamin
• 2,2-Dimetoxyethyl Amine
• AMINOACETALDEHYDE DIMETHYL ACETAL

Aminoacetaldehyde Dimethyl Acetal

CAS: 22483-09-6

Formula: C₄H₁₁NO₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 105.14

Ref: 3B-A0801

Aminoacetaldehyde dimethyl acetal, 99%

CAS: 22483-09-6

Amino acetaldehyde dimethyl was used in preparation of chitosan- dendrimer hybrids having various functional groups such as carboxyl, ester and poly(ethylene glycol). It was used in an synthesis of a bicyclic proline analog from L-ascorbic acid and in 3-component reaction catalyzed by MgClO4 leadin

Formula: C₄H₁₁NO₂

Purity: 99%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 105.14

Ref: 02-A15498

2,2-Dimethoxyethylamine

CAS: 22483-09-6

Formula: C₄H₁₁NO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 105.1356

Ref: IN-DA0037IU

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Aminoacetaldehyde dimethyl acetal

Formula: C₄H₁₁NO₂

Purity: 98%

Color and Shape: clear.colourless liquid

Molecular weight: 105.13564g/mol

Ref: 54-OR4745

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Formula: H₂NCH₂CH(OCH₃)₂

Purity: ≥ 98.0%

Color and Shape: Clear, colourless to light yellow liquid

Molecular weight: 105.14

Ref: 7W-GK6848

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Formula: C₄H₁₁NO₂

Purity: 98%

Color and Shape: Liquid, Colourless liquid

Molecular weight: 105.137

Ref: 10-F094452

Glycinal Dimethyl Acetal

Controlled Product

CAS: 22483-09-6

Applications Glycinal Dimethyl Acetal, is a versatile building block used for the synthesis of various pharmaceutical compounds. It can be used for the preparation a series of novel pyrazolo[1,5-a]pyrazine derivatives.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Zaremba, O. V., et al.: Chem. Heterocyclic Comp., 49, 915 (2013);

Formula: C₄H₁₁NO₂

Color and Shape: Neat

Molecular weight: 105.14

Ref: TR-G616495

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Aminoacetaldehyde dimethyl acetal (ADMA) is a molecule that binds to the receptor protein and has a biological action. ADMA is synthesized by reacting an amide with a reactive solution containing nitrogen atoms. The reaction proceeds through elimination of water, which forms an acetal. This compound can be used for the analysis of amines and other compounds that contain hydroxyl groups. The analytical chemistry of ADMA involves reactions such as acid hydrolysis, esterification, and reduction. A possible reaction mechanism for this molecule includes the formation of an acetic acid derivative from trifluoroacetic acid, which reacts with dopamine β-hydroxylase to form an acetal.

Formula: C₄H₁₁NO₂

Purity: Min. 99.00%

Color and Shape: Clear Liquid

Molecular weight: 105.14 g/mol

Ref: 3D-FA52497