Home > Compound List > Compound details
190970-57-1 molecular structure
click picture or here to close

(4S)-4-phenyl-1,3-oxazolidine-2-thione

ChemBase ID: 77299
Molecular Formular: C9H9NOS
Molecular Mass: 179.23886
Monoisotopic Mass: 179.04048491
SMILES and InChIs

SMILES:
N1C(=S)OC[C@@H]1c1ccccc1
Canonical SMILES:
S=C1OC[C@@H](N1)c1ccccc1
InChI:
InChI=1S/C9H9NOS/c12-9-10-8(6-11-9)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,10,12)/t8-/m1/s1
InChIKey:
LVIJIGQKFDZTNC-MRVPVSSYSA-N

Cite this record

CBID:77299 http://www.chembase.cn/molecule-77299.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(4S)-4-phenyl-1,3-oxazolidine-2-thione
IUPAC Traditional name
(4S)-4-phenyl-1,3-oxazolidine-2-thione
Synonyms
(S)-4-Phenyl-1,3-oxazolidine-2-thione
(S)-4-Phenyloxazolidine-2-thione
(S)-4-苯基噁唑烷-2-硫酮
CAS Number
190970-57-1
MDL Number
MFCD06658219
PubChem SID
24846233
162042172
PubChem CID
11286808

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 11286808 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.587312  H Acceptors
H Donor LogD (pH = 5.5) 2.314949 
LogD (pH = 7.4) 2.2911336  Log P 2.3152637 
Molar Refractivity 51.2909 cm3 Polarizability 20.409678 Å3
Polar Surface Area 21.26 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Optical Rotation
[α]/D +77±3°, c = 0.2 in chloroform expand Show data source
Storage Warning
Irritant expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Purity
≥98.0% expand Show data source
Optical Purity
enantiomeric ratio: ≥99.0:1.0 (LC) expand Show data source
Empirical Formula (Hill Notation)
C9H9NOS expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 08913 external link
Application
A highly selective and efficient chiral auxiliary1 which can be directly reduced to its corresponding aldehyde and the chiral auxiliary by reductive cleavage with diisobutylaluminum hydride.2
Evans-Type Oxazolidinethione And Thiazolidinethione Auxiliaries

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