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60864-26-8 molecular structure
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diiodothulium

ChemBase ID: 144516
Molecular Formular: I2Tm
Molecular Mass: 422.74315
Monoisotopic Mass: 422.743159
SMILES and InChIs

SMILES:
I[Tm]I
Canonical SMILES:
I[Tm]I
InChI:
InChI=1S/2HI.Tm/h2*1H;/q;;+2/p-2
InChIKey:
XGGRJQVPUOEAEU-UHFFFAOYSA-L

Cite this record

CBID:144516 http://www.chembase.cn/molecule-144516.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
diiodothulium
IUPAC Traditional name
diiodothulium
Synonyms
Thulium(II) iodide
碘化铥(II)
CAS Number
60864-26-8
MDL Number
MFCD08276776
PubChem SID
162238729
24883940
PubChem CID
5231385

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
653268 external link Add to cart Please log in.
Data Source Data ID
PubChem 5231385 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 1.8672  LogD (pH = 7.4) 1.8672 
Log P 1.8672  Molar Refractivity 26.6816 cm3
Polarizability 18.68906 Å3 Polar Surface Area 0.0 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
powder expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Purity
≥99.9% expand Show data source
Grade
anhydrous expand Show data source
Linear Formula
TmI2 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 653268 external link
Application
Promotes the cross-coupling of 2-acetylthiophene or ethyl 2-thiophenecarboxylate with aldehydes and ketones in THF at room temperature.1
Features and Benefits
Reducing agent similar to SmI2
Packaging
1 g in ampule

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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