66304-01-6
66304-01-6
Chemical Structure
Beaucage reagent
- CAS No.: 66304-01-6
- Formula:C7H4O3S2
- Molecular Weight:200.24
IUPAC Name: 3H-benzo[c][1,2]dithiol-3-one 1,1-dioxide
InChIKey: JUDOLRSMWHVKGX-UHFFFAOYSA-N
SMILES: O=C(C1=CC=CC=C12)SS2(=O)=O
Biological Activity: Beaucage reagent is found to be potent in causing DNA cleavage[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Beaucage reagent | 98.0% | Beaucage reagent is found to be potent in causing DNA cleavage. | ||||||||||||||||||||
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Beaucage reagent (Standard) | ≥98% | Beaucage reagent (Standard) is the analytical standard of Beaucage reagent (HY-100951). This product is intended for research and analytical applications. Beaucage reagent is found to be potent in causing DNA cleavage. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.83
HY-W777496Saccharin-13C6 -
Similarity Score 0.83
HY-Y0272Saccharin -
Similarity Score 0.64
HY-W010058R2-Methylbenzenesulfonamide (Standard) -
Similarity Score 0.63
HY-W015302R2-Aminobenzenesulfonic acid (Standard) -
Similarity Score 0.63
HY-W012669RPhthalaldehyde (Standard) -
Similarity Score 0.63
HY-Y1771R2-Carboxybenzaldehyde (Standard) -
Similarity Score 0.63
HY-I0508Phthalic acid -
Similarity Score 0.63
HY-W782213Phthalic acid-13C -
Similarity Score 0.62
HY-W134389Potassium p-toluenethiosulfonate, 98% -
Explore the MedChemAI to find more analogs
References
- [1]. Zheng J, et al. Thiol-dependent DNA cleavage by aminomethylated Beaucage's reagent. Org Biomol Chem. 2010 Mar 21;8(6):1293-5. [Content Brief]
- [2]. C. F. H. Allen, et al. Working with Hazardous Chemicals. Organic Syntheses, Coll. Vol. 2, 1943, 580.
- [3]. Stec W J, et al. Bis (O, O-diisopropoxy phosphinothioyl) disulfide-a highly efficient sulfurizing reagent for cost-effective synthesis of oligo (nucleoside phosphorothioate) s[J]. Tetrahedron letters, 1993, 34(33): 5317-5320.
