Aminoacetaldehyde dimethyl acetal - CAS 22483-09-6

Name: Aminoacetaldehyde dimethyl acetal
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB017636
Product Name:	Aminoacetaldehyde dimethyl acetal
CAS:	22483-09-6
Synonyms:	Ethanamine, 2,2-dimethoxy-; Ethylamine, 2,2-dimethoxy-; 1-Amino-2,2-dimethoxyethane; 1-Amino-2,2-dimethyloxyethane; 2,2-Dimethoxyethan-1-amine; 2,2-Dimethoxyethylamine; 2-Aminoacetaldehyde dimethyl acetal; Aminoacetaldehyde dimethylacetal; DEA; Glycinal dimethyl acetal; N-(2,2-Dimethoxyethyl)amine; NSC 73701

Technical Data

Related CAS:	1005473-07-3 (Deleted CAS)
IUPAC Name:	2,2-dimethoxyethanamine
Description:	Aminoacetaldehyde dimethyl acetal (CAS# 22483-09-6) 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.
Molecular Weight:	105.14
Molecular Formula:	C4H11NO2
Canonical SMILES:	COC(CN)OC
InChI:	InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3
InChI Key:	QKWWDTYDYOFRJL-UHFFFAOYSA-N
Boiling Point:	137-139°C
Melting Point:	-78 °C
Purity:	95%
Density:	0.9676 g/cm³
Solubility:	Soluble in Chloroform, Methanol
Appearance:	Clear, colourless to slightly yellowish liquid
Storage:	Store at 2-8°C
MDL:	MFCD00008135
LogP:	0.26430

GHS Hazard Statement:	H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]
Precautionary Statement:	P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, and P501
Signal Word:	Danger

Publication Number	Title	Priority Date
CN-113480481-A	Preparation method of degradation impurities in ivabradine hydrochloride	20210721
CN-113480441-A	Method for preparing aminoacetaldehyde dialkyl acetal	20210615
CN-112946143-A	Analysis and detection method of 7, 8-dimethoxy-1, 3-dihydro-2H-3-benzazepin-2-ketone	20210316
KR-102295216-B1	Metal mask detergent composition and the method thereof	20210302
CN-112500336-A	Preparation method of dolutegravir mother nucleus intermediate	20201215

PMID	Publication Date	Title	Journal
17971730	20060809	1,4-Benzodiazepine N-nitrosoamidines: useful intermediates in the synthesis of tricyclic benzodiazepines	Molecules (Basel, Switzerland)
16602718	20060401	Dendritic saccharide surfactant polymers as antifouling interface materials to reduce platelet adhesion	Biomacromolecules
16140019	20051201	New 1,2,3,4-tetrahydro-1-aza-anthraquinones and 2-aminoalkyl compounds from norlapachol with molluscicidal activity	Bioorganic & medicinal chemistry
9511457	19970701	Synthesis of N-(6-chloro-7-R-1,1-dioxo-1,4,2-benzodithiazin-3- yl)aminoacetaldehyde dimethyl acetals and their transformations into 8-chloroimidazo [1,2-b][1,4,2]benzodithiazine 5,5-dioxide derivatives with potential anti-HIV or anticancer activity	Acta poloniae pharmaceutica

Complexity:	36.7
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	105.078978594
Formal Charge:	0
Heavy Atom Count:	7
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	105.078978594
Rotatable Bond Count:	3
Topological Polar Surface Area:	44.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-0.8