1-Aminonaphthalene-3,6,8-trisulfonic acid | CAS:117-42-0
1-Aminonaphthalene-3,6,8-trisulfonic acid
- Name：1-Aminonaphthalene-3,6,8-trisulfonic acid
- CAS：117-42-0
- Synonyms：1-Naphthylamine-3,6,8-trisulfonic acid; 3,6,8-Trisulfo-1-naphthylamine; 8-Aminonaphthalene-1,3,6-trisulfonic acid; Amino-H acid; Koch acid; Koch's acid; NSC 227195; T Acid
- Molecular Formula：C10H9NO9S3
- Molecular Weight：383.38
- EINESC：204-188-7
Description
Properties
| Density | 1.974 |
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Safety
| 没有数据 | 没有数据 |
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SDS
| Source | SDS/MSDS Samples |
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| 没有数据 | 没有数据 |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
Synthesis of some novel ?-spiroiminolactones from reaction of cyclohexyl isocyanide and dialkyl acetylene dicarboxylates with 1-benzylisatin and tryptanthrine.Azizian J, et al. Synthetic Communications, 33(3), 387-391 (2003)
Nanomolar Synthesis in Droplet Microarrays with UV-Triggered On-Chip Cell Screening.Marius Brehm et al.Small (Weinheim an der Bergstrasse, Germany), 16(10), e1905971-e1905971 (2020-01-28)
On-site fabrication of injectable 131I-labeled microgels for local radiotherapy.Sodam Kim et al.Journal of controlled release : official journal of the Controlled Release Society, 322, 337-345 (2020-04-05)
Structure and Thermal Isomerization of the Adducts Formed in the Reaction of Cyclohexyl Isocyanide with Dimethyl Acetylenedicarboxylate1.Junjappa H, et al. The Journal of Organic Chemistry, 63(26), 9801-9805 (1998)
Synthesis of 3-(Cyclohexylamino)-2-arylimidazo[1,2-a]pyridine-8- carboxylic Acids Via an Efficient Three-component Condensation Reaction between Cyclohexylisocyanide and 2-Aminopyridine-3-carboxylic Acid in the Presence of Aromatic Aldehyde.Ghasem Marandi Combinatorial chemistry & high throughput screening, 21(4), 298-301 (2018-04-18)
Remarks
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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