1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE CAS 128244-01-9

Introduction:Basic information about 1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE CAS 128244-01-9, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Basic information

Product Name:1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE
Synonyms:1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE;1,7-Diazaspiro[4.4]nonane, 1-(phenylMethyl)-;1-Benzyl-1,7-diazaspiro[4.4]nonane heMioxalte;1-Benzyl-1,7-diazaspiro[4.4]nonane hemioxalate, 95%
CAS:128244-01-9
MF:C14H20N2
MW:216.32
EINECS:
Product Categories:
Mol File:128244-01-9.mol

1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Chemical Properties

Boiling point 328.1±17.0 °C(Predicted)
density 1.08±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.68±0.20(Predicted)

Safety Information

Risk Statements 36/37/38
Safety Statements 26-36
HS Code 29339900

1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Usage And Synthesis

SynthesisThe synthesis of the 1-benzyl-1,7-diazaspiro[4,4]nonane core structure (a spirocyclic diamine structure) typically involves a multi-step reaction to construct two fused pyrrolidine rings sharing a single spirocyclic carbon atom. A common approach is to utilize suitable linear or pre-cyclized precursors for reductive amination or cyclization. For example, the synthesis can begin with a protected diamine derivative followed by a key step, such as an intramolecular cyclization of a linear intermediate containing a primary amine and an electrophilic center (e.g., a toluenesulfonate or halide), to form one of the pyrrolidine rings. The second ring forms the spirocyclic center, typically constructed via a subsequent cyclization reaction or a [3+2] cycloaddition reaction. The final step is the introduction of a benzyl group, usually through N-alkylation of the secondary amine with benzyl bromide or benzyl chloride, or reductive amination with benzaldehyde, followed by removal of the remaining protecting group to yield 1-benzyl-1,7-diazaspiro[4.4]nonane.

1-BENZYL-1,7-DIAZASPIRO[4,4]NONANE Preparation Products And Raw materials

1-Benzhydrylazetane-3-carbonitrile CAS 36476-86-5
1-BENZYL-3-P-TOLYLTRIAZENE CAS 17683-09-9
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