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145588-94-9 molecular structure
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(4S)-4-benzyl-1,3-oxazolidine-2-thione

ChemBase ID: 77302
Molecular Formular: C10H11NOS
Molecular Mass: 193.26544
Monoisotopic Mass: 193.05613498
SMILES and InChIs

SMILES:
N1[C@H](COC1=S)Cc1ccccc1
Canonical SMILES:
S=C1OC[C@@H](N1)Cc1ccccc1
InChI:
InChI=1S/C10H11NOS/c13-10-11-9(7-12-10)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,13)/t9-/m0/s1
InChIKey:
WJSUXYCBZFLXIK-VIFPVBQESA-N

Cite this record

CBID:77302 http://www.chembase.cn/molecule-77302.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(4S)-4-benzyl-1,3-oxazolidine-2-thione
IUPAC Traditional name
(4S)-4-benzyl-1,3-oxazolidine-2-thione
Synonyms
(R)-4-Benzyl-1,3-oxazolidine-2-thione
(S)-4-Benzyloxazolidine-2-thione
(S)-4-苄基噁唑烷-2-硫酮
CAS Number
145588-94-9
MDL Number
MFCD06658222
MFCD06658221
PubChem SID
24846176
162042175
PubChem CID
11095486

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 11095486 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.69626  H Acceptors 0 
H Donor 1  LogD (pH = 5.5) 2.6036801 
LogD (pH = 7.4) 2.5850039  Log P 2.603925 
Molar Refractivity 56.0459 cm3 Polarizability 22.257917 Å3
Polar Surface Area 21.26 Å2 Rotatable Bonds 2 
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
63-67 °C 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
≥97.0% expand Show data source
Optical Purity
enantiomeric excess: ≥98.0% (HPLC) expand Show data source
Empirical Formula (Hill Notation)
C10H11NOS expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 08416 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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