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164235113 molecular structure
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[4-(methanesulfonylsulfanyl)butyl]trimethylazanium bromide

ChemBase ID: 179203
Molecular Formular: C8H20BrNO2S2
Molecular Mass: 306.2839
Monoisotopic Mass: 305.01188289
SMILES and InChIs

SMILES:
C(CCCSS(=O)(=O)C)[N+](C)(C)C.[Br-]
Canonical SMILES:
C[N+](CCCCSS(=O)(=O)C)(C)C.[Br-]
InChI:
InChI=1S/C8H20NO2S2.BrH/c1-9(2,3)7-5-6-8-12-13(4,10)11;/h5-8H2,1-4H3;1H/q+1;/p-1
InChIKey:
QQFKXBSXKKHZDG-UHFFFAOYSA-M

Cite this record

CBID:179203 http://www.chembase.cn/molecule-179203.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[4-(methanesulfonylsulfanyl)butyl]trimethylazanium bromide
IUPAC Traditional name
[4-(methanesulfonylsulfanyl)butyl]trimethylazanium bromide
Synonyms
MTSBT
[4-(Trimethylammonium)butyl] Methanethiosulfonate Bromide
PubChem SID
164235113
PubChem CID
57370116

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC T795840 external link Add to cart
PubChem 57370116 external link
Data Source Data ID Price
TRC
T795840 external link Add to cart Please log in.
Data Source Data ID
PubChem 57370116 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) -3.6538384  LogD (pH = 7.4) -3.6538384 
Log P -3.6538384  Molar Refractivity 70.9554 cm3
Polarizability 24.245428 Å3 Polar Surface Area 34.14 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
DMSO expand Show data source
Ethanol expand Show data source
Methanol expand Show data source
Apperance
White Solid expand Show data source
Melting Point
124-125°C expand Show data source
Storage Warning
Moisture Sensitive expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - T795840 external link
Reacts specifically and rapidly with thiols to form mixed disulfides. Used to probe the structures of the ACh receptor channel of the GABAA receptor channel and of lactose permease.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Duhten, R.L., et al.: Biochemistry, 32, 3139 (1993)
  • • Yang, N. et al.: Neuron, 16, 113 (1993)
  • • Kuner, T. et al.: Neuron, 17, 343 (1993)
  • • Holmgren, M. et al: Neuropharmacology, 35, 797 (1993)
  • • Chahine, M. et al.: Biochemical & Biophysical Res. Commun., 233
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PATENTS

PATENTS

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INTERNET

INTERNET

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