CAS 148861-07-8

(T-4)-Triethyl(1,3-propanediamine-κN)boron

Description:

(T-4)-Triethyl(1,3-propanediamine-κN)boron, with the CAS number 148861-07-8, is a chemical compound that features a boron atom coordinated to a triethyl group and a 1,3-propanediamine ligand. This compound is characterized by its coordination chemistry, where the nitrogen atoms of the diamine can act as Lewis bases, forming stable complexes with boron. The presence of triethyl groups contributes to its steric bulk, influencing its reactivity and solubility in organic solvents. Typically, compounds of this nature are utilized in various applications, including catalysis and materials science, due to their ability to facilitate chemical reactions and stabilize reactive intermediates. Additionally, the presence of nitrogen in the structure may impart unique properties, such as potential biological activity or interaction with other chemical species. Overall, (T-4)-Triethyl(1,3-propanediamine-κN)boron exemplifies the diverse functionalities of organoboron compounds in synthetic chemistry.

Formula: C₉H₂₅BN₂

InChI: InChI=1S/C9H25BN2/c1-4-10(5-2,6-3)12-9-7-8-11/h4-9,11-12H2,1-3H3

InChI key: InChIKey=NMWMOBJXEQKUNR-UHFFFAOYSA-N

SMILES: [B+3]([NH2]CCCN)([CH2-]C)([CH2-]C)[CH2-]C

Synonyms:

• Boron, triethyl(1,3-propanediamine-N)-, (T-4)-
• Triethylborane 1,3-diaminopropane complex
• Boron, triethyl(1,3-propanediamine-κN)-, (T-4)-
• (T-4)-Triethyl(1,3-propanediamine-κN)boron
• TEB-DAP

CALLERY™ Triethylborane-1,3-diaminopropane, min. 97%

CAS: 148861-07-8

Formula: (C₂H₅)₃BNH₂(CH₂)₃NH₂

Purity: min. 97%

Color and Shape: colorless to amber

Molecular weight: 172.12

Ref: 08-05-0555

1-(Triethyl-λ4-Boranyl)Propane-1,3-Diamine

CAS: 148861-07-8

1-(Triethyl-λ4-Boranyl)Propane-1,3-Diamine

Purity: 98%

Molecular weight: 171.11g/mol

Ref: 54-OR1027088

Triethylborane-1,3-diaminopropane

CAS: 148861-07-8

Triethylborane-1,3-diaminopropane is a polyolefin radiation initiator. It can be used in the production of polypropylene and polyethylene by polymerizing olefins, such as 2-methylanthraquinone, at low energy. This method has been shown to give photocurable polyolefin plastics with benzophenones and coumarin as substrates. The bonding properties of triethylborane-1,3-diaminopropane are due to its ability to form covalent bonds with the unsaturated groups on the substrate molecules.

Formula: C₉H₂₅BN₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 172.12 g/mol

Ref: 3D-FT178891