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ChemicalBook--->CAS DataBase List--->175217-20-6

175217-20-6

175217-20-6 Structure

175217-20-6 Structure
IdentificationBack Directory
[Name]

SILTHIOFAM
[CAS]

175217-20-6
[Synonyms]

LATITUDE
MON65500
SILTHIOFAM
Silthiopham
Silthiofarm
silthiofam 98%
Silthiofam [iso]
C16947000 Silthiofam
silthiofam (bsi,iso)
Silthiofam, 10 μg /μL in hexane
Silthiofam 100 μg/ml Ethyl acetate
Aldicarb Impurity 4-d3 (Butocarboxim-d3)
L16947000CY Silthiofam 10μg/mLin Cyclohexane
N-Allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide
4,5-Dimethyl-N-2-propenyl-2-(trimethylsilyl)-3-thiophenecarboxamide
3-Thiophenecarboxamide, 4,5-dimethyl-N-2-propenyl-2-(trimethylsilyl)-
3-Thiophenecarboxamide, 4,5-dimethyl-N-2-propen-1-yl-2-(trimethylsilyl)-
[Molecular Formula]

C13H21NOSSi
[MDL Number]

MFCD04112621
[MOL File]

175217-20-6.mol
[Molecular Weight]

267.46
Chemical PropertiesBack Directory
[Boiling point ]

303.2±42.0 °C(Predicted)
[density ]

1.01±0.1 g/cm3(Predicted)
[Fp ]

12°C
[form ]

neat
[pka]

15.11±0.46(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS08,GHS09
[Signal word ]

Warning
[Hazard statements ]

H373-H411
[Precautionary statements ]

P260-P273-P314-P391-P501
[Risk Statements ]

52/53
[Safety Statements ]

61
[RIDADR ]

UN1219 - class 3 - PG 2 - Isopropanol
[WGK Germany ]

1
[RTECS ]

NT8050000
Hazard InformationBack Directory
[Uses]

Silthiofam is a fungicide. It is derived from 3-Chloro-2-butanone (C366895), which is widely used in the chemical and pharmaceutical industries as an intermediate or starting material (for example its use in a one-pot synthesis of γ-iminolactones). Also, it is derived from 2-Amino-4,5-dimethyl-3-thiophenecarboxylic Acid Ethyl Ester (A605165), which is used in the preparation triazine and pyrimidine derivatives as anti-inflammatory and analgesic agents. Also used in the synthesis of antioxidants through heteroaryl amines as well as CB2 cannabinoid receptor partial agonists.
[Definition]

ChEBI: 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'.
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