CAS 22483-09-6

Acetaldeide amminoacetale dimetilico

Descrizione:

Acetaldeide amminoacetale dimetilico, con il numero CAS 22483-09-6, è un composto organico caratterizzato dal suo gruppo funzionale acetalico, che si forma dalla reazione di un aldeide con alcoli. Questo composto appare tipicamente come un liquido incolore o giallo pallido e ha un odore distintivo. È solubile in solventi organici e presenta una stabilità moderata in condizioni standard. La presenza del gruppo amminico suggerisce una reattività potenziale in varie reazioni chimiche, comprese le sostituzioni nucleofile e le reazioni di condensazione. Acetaldeide amminoacetale dimetilico è spesso utilizzato come intermedio nella sintesi di prodotti farmaceutici e agrochimici, grazie alla sua capacità di partecipare a ulteriori trasformazioni chimiche. Inoltre, potrebbe avere applicazioni nella produzione di prodotti chimici speciali e come blocco di costruzione nella sintesi organica. Devono essere osservate precauzioni di sicurezza quando si maneggia questo composto, poiché potrebbe comportare rischi per la salute se inalato o ingerito, e deve essere utilizzato un adeguato equipaggiamento di protezione personale.

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

Sinonimi:

• 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

Purezza: >98.0%(GC)(T)

Colore e forma: Colorless to Almost colorless clear liquid

Peso molecolare: 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

Purezza: 99%

Colore e forma: Clear colorless to pale yellow, Liquid

Peso molecolare: 105.14

Ref: 02-A15498

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Aminoacetaldehyde dimethyl acetal

Formula: C₄H₁₁NO₂

Purezza: 98%

Colore e forma: colourless - yellow Liquid

Peso molecolare: 105.13564

Ref: 54-OR4745

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Formula: H₂NCH₂CH(OCH₃)₂

Purezza: ≥ 98.0%

Colore e forma: Clear, colourless to light yellow liquid

Peso molecolare: 105.14

Ref: 7W-GK6848

2,2-Dimethoxyethanamine

CAS: 22483-09-6

2,2-Dimethoxyethanamine

Formula: C₄H₁₁NO₂

Purezza: 98%

Peso molecolare: 105.14

Ref: IN-DG40872

Aminoacetaldehyde dimethyl acetal

CAS: 22483-09-6

Formula: C₄H₁₁NO₂

Purezza: 98%

Colore e forma: Liquid, Colourless liquid

Peso molecolare: 105.137

Ref: 10-F094452

Glycinal Dimethyl Acetal

Prodotto controllato

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

Colore e forma: Neat

Peso molecolare: 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

Purezza: Min. 99.00%

Colore e forma: Clear Liquid

Peso molecolare: 105.14 g/mol

Ref: 3D-FA52497

2,2-Dimethoxyethylamine

CAS: 22483-09-6

Formula: C₄H₁₁NO₂

Purezza: 98%

Colore e forma: Liquid

Peso molecolare: 105.1356

Ref: IN-DA0037IU