Silthiofam

Base Information Edit

Chemical Name:Silthiofam
CAS No.:175217-20-6
Molecular Formula:C₁₃H₂₁NOSSi
Molecular Weight:267.467
Hs Code.:
European Community (EC) Number:605-752-9
UNII:5991I541GW
DSSTox Substance ID:DTXSID1058000
Nikkaji Number:J1.067.650I
Wikidata:Q18630756
ChEMBL ID:CHEMBL2288019
Mol file:175217-20-6.mol

Synonyms:silthiofam

Suppliers and Price of Silthiofam

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
Silthiofam
2.5mg
$ 460.00

TRC
Silthiofam
10mg
$ 595.00

Sigma-Aldrich
Silthiofam PESTANAL
25mg
$ 238.00

Arctom
N-Allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide
1g
$ 744.00

American Custom Chemicals Corporation
LATITUDE 98.00%
100ML
$ 2739.00

Adipogen Life Sciences
Silthiopham ≥98%(HPLC)
25 mg
$ 129.00

Total 11 raw suppliers

Chemical Property of Silthiofam Edit

Chemical Property:

Vapor Pressure:0.001mmHg at 25°C
Refractive Index:1.513
Boiling Point:303.2°Cat760mmHg
Flash Point:137.2°C
PSA：57.34000
Density:1.01g/cm³
LogP:3.21680
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:267.11131200
Heavy Atom Count:17
Complexity:300

Purity/Quality:

98%,99%, ^*data from raw suppliers

Silthiofam ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 52/53
Safety Statements: 61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC1=C(SC(=C1C(=O)NCC=C)[Si](C)(C)C)C
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.

Technology Process of Silthiofam

There total 8 articles about Silthiofam which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.6%

: C₁₀H₁₅ClOSSi

: 107-11-9,30551-89-4
1-amino-2-propene

: 175217-20-6
silthiofam

Guidance literature:: C₁₀H₁₅ClOSSi; 1-amino-2-propene; In n-heptane; at 20 - 45 ℃; for 0.416667h; Industrial scale;

With sodium hydroxide; In n-heptane; water; at 45 - 50 ℃; for 0.333333h; Industrial scale;
DOI:10.1021/op020206f