1. Home
  2. Ethanamine, 2,2-dimethoxy-N,N-dimethyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Ethanamine, 2,2-dimethoxy-N,N-dimethyl-

COC(CN(C)C)OC Request for Quotation
Chemical Name: Ethanamine, 2,2-dimethoxy-N,N-dimethyl-
CAS Number: 38711-20-5
Product Number: AG0034RH(AGN-PC-0JLOGZ)
Synonyms:
MDL No: MFCD00010205
Molecular Formula: C6H15NO2
Molecular Weight: 133.1888

Identification/Properties

Properties
BP:
165.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Moisture Sensitive
Refractive Index:
1.4060-1.4100
Computed Properties
Molecular Weight:
133.191g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
133.11g/mol
Monoisotopic Mass:
133.11g/mol
Topological Polar Surface Area:
21.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
62.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1993
Hazard Statements:
H226-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Dimethylaminoacetaldehyde Dimethylacetal is a versatile compound commonly used in chemical synthesis. It serves as a valuable building block in the creation of various organic molecules due to its unique properties and reactivity. One of the key applications of Dimethylaminoacetaldehyde Dimethylacetal is its use as a reagent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. This compound is particularly useful in organic transformations such as nucleophilic additions, Mannich-type reactions, and reductive aminations. Additionally, Dimethylaminoacetaldehyde Dimethylacetal can be employed in the preparation of complex molecules with multiple stereocenters, making it an indispensable tool for synthetic chemists working in drug discovery and material science. Its ability to introduce functional groups and modify molecular structures with high efficiency and selectivity makes Dimethylaminoacetaldehyde Dimethylacetal a valuable component in the toolbox of any synthetic chemist.