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Available Variants1 g
CHA.45872-1g
Price
€50.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.45872-1g | €50.80 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C4H5N3S |
|---|---|
| CAS Number | 333-49-3 |
| Molecular Weight | 127.17 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 329752415 |
| EC Number | 206-374-3 |
| Beilstein/REAXYS Number | 112435 |
| MDL number | MFCD00057341 |
| Assay | 97% |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
2-Thiocytosine, also known as 2-mercaptocytosine, is a sulfur-containing nucleobase analog with the CAS registry number 333-49-3. This compound has been studied for its potential therapeutic applications, particularly in the field of oncology. As a structural analog of the naturally occurring nucleobase cytosine, 2-thiocytosine can be incorporated into nucleic acids, where it may exert cytotoxic effects on rapidly dividing cancer cells. The mechanism of action of 2-thiocytosine is thought to involve interference with DNA synthesis and function, leading to cell cycle arrest and apoptosis in susceptible cells. Further research is needed to fully elucidate the pharmacological properties and potential clinical uses of 2-thiocytosine, but its unique chemical structure and biological activity make it an interesting candidate for development as an anticancer agent. Its chemical properties and reactivity are also of interest in various biochemical studies.
