ALD00108
3,6-Bis(methylthio)-1,2,4,5-tetrazine
≥95% (HPLC)
Synonym(s):
3,6-Bis(methylthio)-s-tetrazine, NSC 674352, s-Tetrazine
About This Item
Recommended Products
![3-(([1,1′-Biphenyl]-4-ylmethyl)thio)-6-methyl-1,2,4,5-tetrazine >98%](/deepweb/assets/sigmaaldrich/product/structures/641/985/7d39c434-c9ea-490e-974f-7653ca3b9e8c/640/7d39c434-c9ea-490e-974f-7653ca3b9e8c.png)
Quality Level
Assay
≥95% (HPLC)
form
powder
mp
82-87 °C
storage temp.
−20°C
SMILES string
CSC1=NN=C(SC)N=N1
InChI
1S/C4H6N4S2/c1-9-3-5-7-4(10-2)8-6-3/h1-2H3
InChI key
ROUDTSAXQIBBFZ-UHFFFAOYSA-N
Application
It can also used to synthesize:
- Substituted indoles and indolines derivatives by sequential [4+2] cycloaddition reactions.
- 3-(Methylthio)-6-(4-morpholinyl)-1,2,4,5-tetrazine by aromatic nucleophilic substitution reaction.
related product
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
Inverse electron demand Diels-Alder reactions enable total synthesis of natural products with heteroaromatic ring systems.
Inverse electron demand Diels-Alder reactions enable total synthesis of natural products with heteroaromatic ring systems.
Inverse electron demand Diels-Alder reactions enable total synthesis of natural products with heteroaromatic ring systems.
Inverse electron demand Diels-Alder reactions enable total synthesis of natural products with heteroaromatic ring systems.
Related Content
As the exploration of the properties of complex natural products becomes increasingly more sophisticated with the technological advances being made in their screening and evaluation and as structural details of their interaction with biological targets becomes more accessible, the importance and opportunities for providing unique solutions to complex biological problems has grown. The Boger Lab addresses these challenging problems by understanding the complex solutions and subtle design elements that nature has provided in the form of a natural product and work to extend the solution through rational design elements to provide more selective, more efficacious, or more potent agents designed specifically for the problem or target under investigation. The resulting efforts have reduced many difficult or intractable synthetic challenges to manageable problems providing an approach not only to the natural product but one capable of simple extrapolation to a series of structural analogs with improved selectivity and efficacy.
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