Key Documents

View All Documentation

756792

3,7-Diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane

Name: 3,7-Diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane
Brand: ALDRICH

97%

Synonym(s):

DAPTA

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₉H₁₆N₃O₂P

CAS Number:

63249-99-0

Molecular Weight:

229.22

NACRES:

NA.22

PubChem Substance ID:

329766617

UNSPSC Code:

12352005

MDL number:

MFCD21608498

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

97%

form

solid

mp

183 °C (decomposition)

functional group

phosphine

SMILES string

CC(=O)N1CN2CN(CP(C2)C1)C(C)=O

InChI

1S/C9H16N3O2P/c1-8(13)11-3-10-4-12(9(2)14)7-15(5-10)6-11/h3-7H2,1-2H3

InChI key

MYJHMDGWZWBLCK-UHFFFAOYSA-N

Description

Application

3,7-Diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane is a phosphine ligand and acetylized derivative of 1,3,5-triaza-7-phosphaadamantane that can be used:

As a ligand in the synthesis of diiron dithiolate complexes of Fe-only hydrogenase to improve the hydro- and protophilicity of the active site.
To prepare (η⁶-arene)-ruthenium(II) complex, which is employed as a catalyst in the reduction of allylic alcohols.
As a ligand in the synthesis of water-soluble cis- and trans-Pt(II) and Pd(II) metal complexes.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

SHBR6159

SHBL8942

SHBB8585

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and characterization of Pt(II) and Pd(II) PTA and DAPTA complexes

Braddock-Wilking J, et al.

Polyhedron, 79(1), 16-28 (2014)

Enriching the Housing Environment for Mice Enhances Their NK Cell Antitumor Immunity via Sympathetic Nerve-Dependent Regulation of NKG2D and CCR5.

Yanfang Song et al.

Cancer research, 77(7), 1611-1622 (2017-01-14)

Mice housed in an enriched environment display a tumor-resistant phenotype due to eustress stimulation. However, the mechanisms underlying enriched environment-induced protection against cancers remain largely unexplained. In this study, we observed a significant antitumor effect induced by enriched environment in

Ruthenium-catalyzed reduction of allylic alcohols using glycerol as solvent and hydrogen donor

Diaz-Alvarez AE, et al.

Catalysis Communications, 13(1), 91-96 (2011)

View All Related Papers

Global Trade Item Number

SKU	GTIN
756792-500MG	04061833230336
756792-2G	04061833339978