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190970-57-1 molecular structure
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(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

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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
162042172
24846233
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 0 
H Donor 1  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 1 
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

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PATENTS

PATENTS

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INTERNET

INTERNET

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