Home > Compound List > Compound details
799297-44-2 molecular structure
click picture or here to close

[(1R,2R)-2-amino-1-phenylpropyl]diphenylphosphane

ChemBase ID: 301554
Molecular Formular: C21H22NP
Molecular Mass: 319.379841
Monoisotopic Mass: 319.14898634
SMILES and InChIs

SMILES:
N[C@@H]([C@@H](c1ccccc1)P(c1ccccc1)c1ccccc1)C
Canonical SMILES:
C[C@H]([C@H](P(c1ccccc1)c1ccccc1)c1ccccc1)N
InChI:
InChI=1S/C21H22NP/c1-17(22)21(18-11-5-2-6-12-18)23(19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-17,21H,22H2,1H3/t17-,21+/m1/s1
InChIKey:
JWZAIGGNEGTDMG-UTKZUKDTSA-N

Cite this record

CBID:301554 http://www.chembase.cn/molecule-301554.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[(1R,2R)-2-amino-1-phenylpropyl]diphenylphosphane
IUPAC Traditional name
[(1R,2R)-2-amino-1-phenylpropyl]diphenylphosphane
Synonyms
(R,R)-(-)-2-Amino-1-phenylpropyldiphenylphosphine
CAS Number
799297-44-2
MDL Number
MFCD17018768

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
Alfa Aesar H60639 external link Add to cart
Data Source Data ID Price
Alfa Aesar
H60639 external link Add to cart Please log in.
Data Source Data ID

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 1.5150652  LogD (pH = 7.4) 2.3154292 
Log P 4.9298  Molar Refractivity 98.5245 cm3
Polarizability 39.40475 Å3 Polar Surface Area 26.02 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
105-109°C expand Show data source
Optical Rotation
-140 (c=0.5 in chloroform) expand Show data source
Storage Warning
Air Sensitive expand Show data source
European Hazard Symbols
Corrosive Corrosive (C) expand Show data source
UN Number
UN3259 expand Show data source
Hazard Class
8 expand Show data source
Packing Group
III expand Show data source
Risk Statements
34 expand Show data source
Safety Statements
20-26-36/37/39-45-60 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS Hazard statements
H314-H318 expand Show data source
GHS Precautionary statements
P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501 expand Show data source
Purity
97+% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle