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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
H Donor 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
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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