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2664-63-3,MFCD00002349
Catalog No.:AA00I4YU

2664-63-3 | Phenol, 4,4'-thiobis-

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
98%
in stock  
$16.00   $12.00
- +
500g
>98.0%(GC)
in stock  
$156.00   $109.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00I4YU
Chemical Name:
Phenol, 4,4'-thiobis-
CAS Number:
2664-63-3
Molecular Formula:
C12H10O2S
Molecular Weight:
218.2716
MDL Number:
MFCD00002349
SMILES:
Oc1ccc(cc1)Sc1ccc(cc1)O
NSC Number:
203030
Properties
Computed Properties
 
Complexity:
162  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.3  

Literature

Title: Activation of G protein-coupled receptor 30 by thiodiphenol promotes proliferation of estrogen receptor α-positive breast cancer cells.

Journal: Chemosphere 20170201

Title: In vitro profiling of toxicity and endocrine disrupting effects of bisphenol analogues by employing MCF-7 cells and two-hybrid yeast bioassay.

Journal: Environmental toxicology 20170101

Title: Influence of the polymer backbone structure on the properties of aromatic ionomers with pendant sulfobenzoyl side chains for use as proton-exchange membranes.

Journal: ACS applied materials & interfaces 20101201

Title: Monocyclic aromatic amines as potential human carcinogens: old is new again.

Journal: Carcinogenesis 20100101

Title: Fabrication of compositional-gradient biodegradable polymeric films showing self-bending deformation.

Journal: Macromolecular rapid communications 20090319

Title: Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.

Journal: Journal of molecular graphics & modelling 20061101

Title: Comparison of the reporter gene assay for ER-alpha antagonists with the immature rat uterotrophic assay of 10 chemicals.

Journal: Toxicology letters 20030430

Title: Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals.

Journal: Toxicology 20030201

Title: Acute toxicity, mutagenicity, and estrogenicity of bisphenol-A and other bisphenols.

Journal: Environmental toxicology 20020201

Title: Transformation of kidney epithelial cells by a quinol thioether via inactivation of the tuberous sclerosis-2 tumor suppressor gene.

Journal: Molecular carcinogenesis 20010501

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SDS
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Tags:2664-63-3 Molecular Formula|2664-63-3 MDL|2664-63-3 SMILES|2664-63-3 Phenol, 4,4'-thiobis-
Catalog No.: AA00I4YU
2664-63-3,MFCD00002349
2664-63-3 | Phenol, 4,4'-thiobis-
Pack Size： 25g
Purity： 98%
in stock
$16.00 $12.00
Pack Size： 500g
Purity： >98.0%(GC)
in stock
$156.00 $109.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA00I4YU
Chemical Name: Phenol, 4,4'-thiobis-
CAS Number: 2664-63-3
Molecular Formula: C12H10O2S
Molecular Weight: 218.2716
MDL Number: MFCD00002349
SMILES: Oc1ccc(cc1)Sc1ccc(cc1)O
NSC Number: 203030
Properties
Complexity: 162  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.3  
Literature fold

Title: Activation of G protein-coupled receptor 30 by thiodiphenol promotes proliferation of estrogen receptor α-positive breast cancer cells.

Journal: Chemosphere20170201

Title: In vitro profiling of toxicity and endocrine disrupting effects of bisphenol analogues by employing MCF-7 cells and two-hybrid yeast bioassay.

Journal: Environmental toxicology20170101

Title: Influence of the polymer backbone structure on the properties of aromatic ionomers with pendant sulfobenzoyl side chains for use as proton-exchange membranes.

Journal: ACS applied materials & interfaces20101201

Title: Monocyclic aromatic amines as potential human carcinogens: old is new again.

Journal: Carcinogenesis20100101

Title: Fabrication of compositional-gradient biodegradable polymeric films showing self-bending deformation.

Journal: Macromolecular rapid communications20090319

Title: Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.

Journal: Journal of molecular graphics & modelling20061101

Title: Comparison of the reporter gene assay for ER-alpha antagonists with the immature rat uterotrophic assay of 10 chemicals.

Journal: Toxicology letters20030430

Title: Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals.

Journal: Toxicology20030201

Title: Acute toxicity, mutagenicity, and estrogenicity of bisphenol-A and other bisphenols.

Journal: Environmental toxicology20020201

Title: Transformation of kidney epithelial cells by a quinol thioether via inactivation of the tuberous sclerosis-2 tumor suppressor gene.

Journal: Molecular carcinogenesis20010501

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