PyBroP

Suppliers

Names

[ Name ]:
PyBroP

[Synonym ]:
PyBrOP;; Bromo-tris-pyrrolidino phosphoniumhexafluorophosphate
Bromo(tripyrrolidin-1-yl)phosphonium hexafluorophosphate
Bromotri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V)
Bromo[tri(pyrrolidin-1-yl)]phosphonium hexafluorophosphate
Bromo-tris-pyrrolidino phosphoniumhexafluorophosphate
Bromo(tri-1-pyrrolidinyl)phosphonium hexafluorophosphate
Bromo-tris-pyrrolidinophosphonium hexafluorophosphate
Bromo-Tris-Pyrrolidinophosphoniumhexafluorophosphate
Bromotripyrrolidinophosphonium hexafluorophosphate
bromo(tripyrrolidin-1-yl)phosphanium,hexafluorophosphate
Bromo-tris-pyrrolidino-phosphonium hexafluorophpsphate
MFCD00077412
PyBroP
BROMO-TRIS-PYRROLIDINO-PHOSPHONIUM HEXAFLUOROPHOSPHATE

Chemical & Physical Properties

[ Melting Point ]:
100 °C

[ Molecular Formula ]:
C₁₂H₂₄BrF₆N₃P₂

[ Molecular Weight ]:
466.18100

[ Exact Mass ]:
465.05300

[ PSA ]:
36.90000

[ LogP ]:
6.54240

[ Storage condition ]:
−20°C

[ Water Solubility ]:
moderately soluble

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

PyBOP
1,1',1''-Phosphoryltripyrrolidine

DownStream

Articles

Non-covalent photo-patterning of gelatin matrices using caged collagen mimetic peptides.

Macromol. Biosci. 15(1) , 52-62, (2015)

To address the downside of conventional photo-patterning which can alter the chemical composition of protein scaffolds, we developed a non-covalent photo-patterning strategy for gelatin (denatured col...

General and mild preparation of 2-aminopyridines.

Org. Lett. 12(22) , 5254-7, (2010)

A general and facile one-pot amination procedure for the synthesis of 2-aminopyridines from the corresponding pyridine-N-oxides is presented as a mild alternative to S(N)Ar chemistry. A variety of ami...

J. Coste et al.

J. Org. Chem. 59 , 2437, (1994)

5-Bromo-2-[(3-methylazetidin-3-yl)oxy]-1,3-thiazole
N-({6-azabicyclo[3.2.1]octan-5-yl}methyl)butanamide
2-(3-Bromopropyl)-1-fluoro-3-methoxy-5-methylbenzene
1-[5-(Aminomethyl)-6-azabicyclo[3.2.1]octan-6-yl]-2,2-dimethylpropan-1-one
{6-Cyclobutanecarbonyl-6-azabicyclo[3.2.1]octan-5-yl}methanamine
1-({6-Azabicyclo[3.2.1]octan-5-yl}methyl)-3-tert-butylurea
1-({6-Azabicyclo[3.2.1]octan-5-yl}methyl)-3-(2-methylpropyl)urea
1-({6-Azabicyclo[3.2.1]octan-5-yl}methyl)-3-(2-methoxyethyl)urea
2-Chloro-5,6,8-trifluoroquinoline-3-carbaldehyde
3-(3-Chloro-2,2-dimethylpropoxy)oxolane

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