Home > Compound List > Compound details
MFCD13193117 molecular structure
click picture or here to close

5-[4-nitro-2-(trifluoromethyl)phenyl]-2H-1,2,3,4-tetrazole

ChemBase ID: 45239
Molecular Formular: C8H4F3N5O2
Molecular Mass: 259.1448696
Monoisotopic Mass: 259.03170905
SMILES and InChIs

SMILES:
c1(nn[nH]n1)c1c(C(F)(F)F)cc([N+](=O)[O-])cc1
Canonical SMILES:
[O-][N+](=O)c1ccc(c(c1)C(F)(F)F)c1n[nH]nn1
InChI:
InChI=1S/C8H4F3N5O2/c9-8(10,11)6-3-4(16(17)18)1-2-5(6)7-12-14-15-13-7/h1-3H,(H,12,13,14,15)
InChIKey:
PQSIDAYQUUYIKI-UHFFFAOYSA-N

Cite this record

CBID:45239 http://www.chembase.cn/molecule-45239.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
5-[4-nitro-2-(trifluoromethyl)phenyl]-2H-1,2,3,4-tetrazole
IUPAC Traditional name
5-[4-nitro-2-(trifluoromethyl)phenyl]-2H-1,2,3,4-tetrazole
Synonyms
5-[4-Nitro-2-(trifluoromethyl)phenyl]-2H-1,2,3,4-tetraazole
MDL Number
MFCD13193117
PubChem SID
162050002
PubChem CID
45588072

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 45588072 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 7.207236  H Acceptors
H Donor LogD (pH = 5.5) 2.7786329 
LogD (pH = 7.4) 2.3974426  Log P 2.786833 
Molar Refractivity 66.7186 cm3 Polarizability 19.069424 Å3
Polar Surface Area 100.28 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
60 - 61 °C expand Show data source
60-61°C expand Show data source
Storage Warning
IRRITANT expand Show data source
MSDS Link
Download expand Show data source
TSCA Listed
false expand Show data source
Purity
>95% expand Show data source

DETAILS

DETAILS

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