Thiophene, 2,3,5-trimethyl-


Chemical Name: Thiophene, 2,3,5-trimethyl-
CAS Number: 1795-05-7
Product Number: AG00271C(AGN-PC-0JLBOD)
Synonyms:
MDL No:
Molecular Formula: C7H10S
Molecular Weight: 126.2193

Identification/Properties


Properties
MP:
-51.23℃ (estimate)
BP:
166.564 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
126.217g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
126.05g/mol
Monoisotopic Mass:
126.05g/mol
Topological Polar Surface Area:
28.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
80.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
1993
Hazard Statements:
H226-H302-H315-H319-H335
Precautionary Statements:
P210-P233-P240-P241-P242-P243-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P303+P361+P353-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P370+P378-P403-P403+P233-P403+P235-P405-P501
Class:
3
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,3,5-Trimethylthiophene is a versatile organic compound that finds wide application in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in the creation of various organic molecules.One of the key uses of 2,3,5-Trimethylthiophene is as a precursor in the synthesis of pharmaceutical compounds. Due to its ability to easily undergo functional group transformations, it is often employed in the preparation of complex drug molecules. Additionally, its presence in certain natural products highlights its significance in medicinal chemistry.Furthermore, 2,3,5-Trimethylthiophene is utilized in the production of agrochemicals and specialty chemicals. Its inclusion in the synthesis of these compounds contributes to enhancing their biological activity and overall efficacy. The distinctive properties of this compound enable chemists to modify its structure effectively, leading to the development of novel chemical entities with diverse applications.In summary, 2,3,5-Trimethylthiophene plays a crucial role in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. Its versatility and reactivity make it a valuable tool for creating a wide range of organic molecules with various functional groups, thus driving innovation and advancement in these fields.