silthiofam
A monocarboxylic acid amide obtained by formal condensation of the carboxy group from 4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxlic acid with the amino group of allylamine. A fungicide seed dressing for cereals used mainly to control 'take-all'.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
-
CHEBI:25713 -
CHEBI:26961 -
CHEBI:29347 - amide fungicide
CHEBI:60600 -
CHEBI:78840
Chemical structure
| Molecular formula | C13H21NOSSi |
|---|---|
| Charge | 0 |
| Average mass | 267.47 Da |
| Monoisotopic mass | 267.11131 Da |
| Source | ChEBI |
| InChIKey | MXMXHPPIGKYTAR-UHFFFAOYSA-N |
C=CCNC(=O)c1c([Si](C)(C)C)sc(C)c1C
InChI=1S/C13H21NOSSi/c1-7-8-14-12(15)11-9(2)10(3)16-13(11)17(4,5)6/h7H,1,8H2,2-6H3,(H,14,15)
Also called
- 4,5-dimethyl-N-(2-propen-1-yl)-2-(trimethylsilyl)thiophene-3-carboxamide
- 4,5-dimethyl-N-2-propen-1-yl-2-(trimethylsilyl)-3-thiophenecarboxamide
- 4,5-dimethyl-N-2-propenyl-2-(trimethylsilyl)-3-thiophenecarboxamide
- N-allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide
- Silthiopham
Cross-references
- cas:175217-20-6
- pesticides:silthiofam
- ppdb:591
- reaxys:11343631
Patents and articles
Activity roles
- fungicide
CHEBI:24127 - antifungal agent
CHEBI:35718 - antifungal agrochemical
CHEBI:86328
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:83393 |
silthiofam | antibioticmech:chebi-0be518635d |
2026-08-30 |
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories