EcoDrugPlus


Keyword(s):	Food Contact Chemicals
Molecule Category	Free-form
EPA CompTox	DTXSID10992442

Keyword(s):

Food Contact Chemicals

Molecule Category

Free-form

EPA CompTox

DTXSID10992442


InChI Key	UYZZVQJHJQMDMM-UHFFFAOYSA-H
Smiles	[F-].[F-].[F-].[F-].[F-].[F-].[Sb+5].CCCCCCCCCCCCC1=CC=C([I+]C2=CC=C(CCCCCCCCCCCC)C=C2)C=C1
InChI	InChI=1S/C36H58I.6FH.Sb/c1-3-5-7-9-11-13-15-17-19-21-23-33-25-29-35(30-26-33)37-36-31-27-34(28-32-36)24-22-20-18-16-14-12-10-8-6-4-2;;;;;;;/h25-32H,3-24H2,1-2H3;6*1H;/q+1;;;;;;;+5/p-6

InChI Key

UYZZVQJHJQMDMM-UHFFFAOYSA-H

Smiles

[F-].[F-].[F-].[F-].[F-].[F-].[Sb+5].CCCCCCCCCCCCC1=CC=C([I+]C2=CC=C(CCCCCCCCCCCC)C=C2)C=C1

InChI

InChI=1S/C36H58I.6FH.Sb/c1-3-5-7-9-11-13-15-17-19-21-23-33-25-29-35(30-26-33)37-36-31-27-34(28-32-36)24-22-20-18-16-14-12-10-8-6-4-2;;;;;;;/h25-32H,3-24H2,1-2H3;6*1H;/q+1;;;;;;;+5/p-6

Property Name	Value
Molecular Formula	C36H58F6ISb
Molecular Weight	852.25
AlogP	-9.62
Number of Rotational Bond	24.0
Heavy Atoms	44.0

Property Name

Value

Molecular Formula

C36H58F6ISb

Molecular Weight

852.25

AlogP

-9.62

Number of Rotational Bond

24.0

Heavy Atoms

44.0

Resources	Reference
CAS NUMBER	71786-70-4
NORMAN SUSDAT
PubChem	91868434

Resources

Reference

CAS NUMBER

71786-70-4

NORMAN SUSDAT

PubChem

91868434


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

BIS(4-DODECYLPHENYL)IODONIUM HEXAFLUOROANTIMONATE

Structure

Physicochemical Descriptors

Cross References