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82358-09-6

82358-09-6 | 2-Thiazolethiol

CAS No: 82358-09-6 Catalog No: AG00ID8I MDL No:MFCD00022449

Product Description

Catalog Number:
AG00ID8I
Chemical Name:
2-Thiazolethiol
CAS Number:
82358-09-6
Molecular Formula:
C3H3NS2
Molecular Weight:
117.1926
MDL Number:
MFCD00022449
IUPAC Name:
3H-1,3-thiazole-2-thione
InChI:
InChI=1S/C3H3NS2/c5-3-4-1-2-6-3/h1-2H,(H,4,5)
InChI Key:
OCVLSHAVSIYKLI-UHFFFAOYSA-N
SMILES:
Sc1nccs1
UNII:
I103PUS4QR

Properties

Complexity:
97  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
116.971g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
117.184g/mol
Monoisotopic Mass:
116.971g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
69.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  

Literature

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Indene-based thiazolidinethione chiral auxiliary for propionate and acetate aldol additions. Organic letters 20080221
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Highly selective acetate aldol additions using mesityl-substituted chiral auxiliaries. Organic letters 20070104
Intestinal-specific PPARgamma deficiency enhances tumorigenesis in ApcMin/+ mice. International journal of cancer 20061115
Double diastereoselective acetate aldol reactions with chiral N-acetyl thiazolidinethione reagents. The Journal of organic chemistry 20060804
Synthesis of (-)-stemoamide using a stereoselective anti-aldol step. The Journal of organic chemistry 20060414
Thiazolidinediones inhibit albumin uptake by proximal tubular cells through a mechanism independent of peroxisome proliferator activated receptor gamma. American journal of nephrology 20060101
Enantioselective synthesis of apoptolidinone: exploiting the versatility of thiazolidinethione chiral auxiliaries. Journal of the American Chemical Society 20051012
On the homolytic cleavage of the N,O bond in N-(methoxy)pyridine-2(1H)-thione and N-(methoxy)thiazole-2(3H)-thione in thermally and photochemically induced reactions: a theoretical study. The journal of physical chemistry. A 20050707
Enantiorecognition on solid chiral selectors using microbatch technology: an example of limitation in case of strong association in the racemate. Biomedical chromatography : BMC 20050701
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Photochemistry of N-isopropoxy-substituted 2(1H)-pyridone and 4-p-tolylthiazole-2(3H)-thione: alkoxyl-radical release (spin-trapping, EPR, and transient spectroscopy) and its significance in the photooxidative induction of DNA strand breaks. The Journal of organic chemistry 20020823
New anti-MRSA and anti-VRE carbapenems; synthesis and structure-activity relationships of 1beta-methyl-2-(thiazol-2-ylthio)carbapenems. The Journal of antibiotics 20020801

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