121967
Aminoacetaldehyde dimethyl acetal
99%
Synonym(s):
2,2-Dimethoxyethylamine
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About This Item
Linear Formula:
NH2CH2CH(OCH3)2
CAS Number:
Molecular Weight:
105.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
245-026-5
Beilstein/REAXYS Number:
741868
MDL number:
Assay:
99%
Quality Segment
assay
99%
refractive index
n20/D 1.417 (lit.)
bp
135-139 °C/95 mmHg (lit.)
density
0.965 g/mL at 25 °C (lit.)
functional group
acetal, amine, ether
SMILES string
COC(CN)OC
InChI
1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3
InChI key
QKWWDTYDYOFRJL-UHFFFAOYSA-N
General description
Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine.
Aminoacetaldehyde dimethyl acetal is used as a building block for the synthesis of various acylated and sufonylated oxyenamides.
Aminoacetaldehyde dimethyl acetal is used as a building block for the synthesis of various acylated and sufonylated oxyenamides.
Application
Aminoacetaldehyde dimethyl acetal was used in a study to develop a fluorescent substrate for aldehyde dehydrogenase. It 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 efficient 3-step synthesis of a bicyclic proline analog from L-ascorbic acid and in 3-component reaction catalyzed by MgClO4 leading to α-aminophosphonates.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
111.2 °F - closed cup
flash_point_c
44 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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