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Home PEG Linkers 942-91-6
942-91-6,MFCD00004927
Catalog No.:AA003U3H

942-91-6 | S-(Thiobenzoyl)thioglycolic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$8.00   $6.00
- +
1g
97%
in stock  
$17.00   $12.00
- +
5g
95%
in stock  
$69.00   $48.00
- +
25g
97%
in stock  
$112.00   $78.00
- +
100g
97%
in stock  
$335.00   $234.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003U3H
Chemical Name:
S-(Thiobenzoyl)thioglycolic acid
CAS Number:
942-91-6
Molecular Formula:
C9H8O2S2
Molecular Weight:
212.2886
MDL Number:
MFCD00004927
SMILES:
S=C(c1ccccc1)SCC(=O)O
Properties
Properties
 
Form:
Solid  
MP:
125-127 °C(lit.)  
Solubility:
acetone: soluble25mg/mL, clear  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
198  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
2.5  

Downstream Synthesis Route

[1]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,2003,vol.42,p.2767-2771

[2]ActaChemicaScandinavica(1947),1952,vol.6,p.957

[1]JournaloftheChemicalSociety.PerkintransactionsI,1981,p.360-365

[2]ArkivfoerKemi,1955,vol.7,p.513

[3]ActaChemicaScandinavica(1947),1961,vol.15,p.1109-1123

[1]Kjaer[ActaChemicaScandinavica(1947),1950,vol.4,p.1347,1349]

[1]JournaloftheChemicalSociety,1957,p.1556,1561

[1]ActaChemicaScandinavica(1947),1950,vol.4,p.1347,1349

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: 2-(Phenyl-carbonothio-ylsulfan-yl)acetic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20101001

Title: Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).

Journal: Bioorganic & medicinal chemistry 20081201

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SDS
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