N-[bis(dimethylamino)boranyl]-n-methylmethanamine - ≥98% , CAS No.4375-83-1

CAS: 4375-83-1 Cat. No.: N136176 Molecular Weight: 143.04 EC Number: 224-474-5

GRADE & PURITY ≥98%

Synonyms

AS-81661 | B(N(CH3)2)3 | Tris(dimethylamino)borane, 99% | N-bis(dimethylamino)boranyl-N-methylmethanamine | AI3-61066 | N-[Bis(dimethylamino)boryl]-N-methylmethanamine # | N,N,N',N',N'',N''-hexamethylboranetriamine | Tris(dimethylamino)borane | N-[bis(dim

Storage

Room temperature

Shipped In

Normal

Overview

Tris(dimethylamino)borane is an organoborane generally used as a macrolactamization reagent. It can also be used to prepare tris(alkylamino)borane analogs by transamination of primary and secondary amines

Reactant involved in:

· B-C-N hybrid films deposited on Ni

· Reduction reactions

· Syntehsis of lithium borom imidazolate framework polymeric complexes

· One-pot oxidative amination

· Synthesis of boron salts and tripodal borate ligands

Specifications

Synonyms

AS-81661 | B(N(CH3)2)3 | Tris(dimethylamino)borane, 99% | N-bis(dimethylamino)boranyl-N-methylmethanamine | AI3-61066 | N-[Bis(dimethylamino)boryl]-N-methylmethanamine # | N, N, N', N', N'', N''-hexamethylboranetriamine | Tris(dimethylamino)borane | N-[bis(dim

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488185507
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185507
• Canonical Smiles: B(N(C)C)(N(C)C)N(C)C
• IUPAC Name: N-[bis(dimethylamino)boranyl]-N-methylmethanamine
• InChIKey: SOLWORTYZPSMAK-UHFFFAOYSA-N
• INCHI: 1S/C6H18BN3/c1-8(2)7(9(3)4)10(5)6/h1-6H3
• Isomeric SMILES: B(N(C)C)(N(C)C)N(C)C
• WGK Germany: 3
• Molecular Weight: 143.04
• Reaxy-Rn: 1738976
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1738976&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic salts
    • Class Organic metal salts
      • Subclass Organic metalloid salts

• Kingdom: Organic compounds
• Superclass: Organic salts
• Class: Organic metal salts
• Subclass: Organic metalloid salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic metalloid salts
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metalloid salt - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Moisture sensitive
• Flash Point(°F): -5.8 °F
• Flash Point(°C): -21 °C
• Boil Point(°C): 147-148°C
• Melt Point(°C): -16 °C
• Molecular Weight: 143.040 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 143.159 Da
• Monoisotopic Mass: 143.159 Da
• Topological Polar Surface Area: 9.700 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 74.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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