(9-Carboxynonyl)(triphenyl)phosphanium bromide

Base Information

Chemical Name:(9-Carboxynonyl)(triphenyl)phosphanium bromide
CAS No.:93943-65-8
Molecular Formula:C28H34O2P.Br
Molecular Weight:513.455
Hs Code.:
ChEMBL ID:CHEMBL3580684
DSSTox Substance ID:DTXSID40596336

Synonyms:93943-65-8;(9-carboxynonyl)triphenylphosphonium bromide;Phosphonium, (9-carboxynonyl)triphenyl-, bromide;(9-Carboxynonyl)(triphenyl)phosphanium bromide;SCHEMBL8091612;CHEMBL3580684;DTXSID40596336;MBBYHWZVGHKEBI-UHFFFAOYSA-N;9-carboxynonyltriphenylphosphonium bromide

Suppliers and Price of (9-Carboxynonyl)(triphenyl)phosphanium bromide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(9-Carboxynonyl)triphenyl-phosphoniumBromide(>90%)
25mg
$ 375.00

Total 0 raw suppliers

Chemical Property of (9-Carboxynonyl)(triphenyl)phosphanium bromide

Chemical Property:

Melting Point:112 - 121°C
PSA：53.72000
LogP:5.80930
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:13
Exact Mass:512.14798
Heavy Atom Count:32
Complexity:442

Purity/Quality:: (9-Carboxynonyl)triphenyl-phosphoniumBromide(>90%) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)[P+](CCCCCCCCCC(=O)O)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
Uses (9-Carboxynonyl)triphenyl-phosphonium Bromide is a compound used to increase the level of hydrogen sulphide within the mitochondria because of the presence of the mitochondria targeting motif (triphenylphosphonium).

Technology Process of (9-Carboxynonyl)(triphenyl)phosphanium bromide

There total 3 articles about (9-Carboxynonyl)(triphenyl)phosphanium bromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 50530-12-6
10-bromodecanoic acid

: 603-35-0
triphenylphosphine

: 93943-65-8
(9-carboxynonyl)triphenylphosphonium bromide

Guidance literature:: at 150 ℃; for 24h;

Reference yield:

: 112-47-0
1,10-Decanediol

: 93943-65-8
(9-carboxynonyl)triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen bromide / toluene / 24 h / 180 °C

2: chromium(VI) oxide; sulfuric acid; water / acetone / -5 - 20 °C

3: toluene / 48 h / Inert atmosphere; Reflux

With chromium(VI) oxide; sulfuric acid; water; hydrogen bromide; In acetone; toluene;
DOI:10.1016/j.bmc.2010.10.060

Reference yield:

: 53463-68-6
1-bromo-10-decanol

: 93943-65-8
(9-carboxynonyl)triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 2 steps

1: chromium(VI) oxide; sulfuric acid; water / acetone / -5 - 20 °C

2: toluene / 48 h / Inert atmosphere; Reflux

With chromium(VI) oxide; sulfuric acid; water; In acetone; toluene;
DOI:10.1016/j.bmc.2010.10.060