PyBroP

Suppliers

Names

[ CAS No. ]:
132705-51-2

[ 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)


More Articles

Related Compounds

  • 2-[({2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-thiazol-4-yl}formamido)oxy]propanoic acid
  • 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-(3-hydroxy-2,2-dimethylpyrrolidin-1-yl)-4-oxobutanoic acid
  • Tert-butyl 2-{[3-(4-bromophenyl)-1-azaspiro[4.5]decan-3-yl]oxy}acetate
  • 7-[3-(Propan-2-yl)phenyl]azepan-2-one
  • 2-(3,3-Dimethylcyclohexyl)-4-(propylamino)butan-1-ol
  • 3-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-methylphenyl]formamido}-3-methylbutanoic acid
  • tert-Butyl (2-((tert-butoxycarbonyl)oxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methoxypropanamido]cyclohexane-1-carboxylic acid
  • 3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-4-hydroxybenzoic acid
  • 2-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-N-propylbutanamido}acetic acid
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.