Home > Compound List > Compound details
MFCD02724565 molecular structure
click picture or here to close

(2E)-2-(1,3-benzothiazol-2-yl)-3-[(2-methylphenyl)amino]-3-sulfanylprop-2-enenitrile

ChemBase ID: 230044
Molecular Formular: C17H13N3S2
Molecular Mass: 323.43522
Monoisotopic Mass: 323.05508943
SMILES and InChIs

SMILES:
c1(/C(=C(\Nc2c(C)cccc2)/S)/C#N)nc2c(s1)cccc2
Canonical SMILES:
N#C/C(=C(/Nc1ccccc1C)\S)/c1nc2c(s1)cccc2
InChI:
InChI=1S/C17H13N3S2/c1-11-6-2-3-7-13(11)19-16(21)12(10-18)17-20-14-8-4-5-9-15(14)22-17/h2-9,19,21H,1H3/b16-12+
InChIKey:
ZMKDQINBDNCVLP-FOWTUZBSSA-N

Cite this record

CBID:230044 http://www.chembase.cn/molecule-230044.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2E)-2-(1,3-benzothiazol-2-yl)-3-[(2-methylphenyl)amino]-3-sulfanylprop-2-enenitrile
IUPAC Traditional name
(2E)-2-(1,3-benzothiazol-2-yl)-3-[(2-methylphenyl)amino]-3-sulfanylprop-2-enenitrile
Synonyms
2-Benzothiazol-2-yl-3-mercapto-3-o-tolylamino-acrylonitrile
MDL Number
MFCD02724565
PubChem SID
164285954
PubChem CID
6098128

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Enamine
EN300-03058 external link Add to cart Please log in.
Data Source Data ID
PubChem 6098128 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 6.9453716  H Acceptors
H Donor LogD (pH = 5.5) 5.077847 
LogD (pH = 7.4) 4.5879173  Log P 5.092328 
Molar Refractivity 103.6856 cm3 Polarizability 36.41537 Å3
Polar Surface Area 48.71 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Product Information Bioassay(PubChem)
Hydrophobicity(logP)
3.907 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