5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine

Base Information

Chemical Name:5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine
CAS No.:50608-12-3
Molecular Formula:C7H13 N3 S
Molecular Weight:171.266
Hs Code.:2934100090
European Community (EC) Number:256-651-8
UNII:8S7FU32R3F
DSSTox Substance ID:DTXSID6068561
Nikkaji Number:J261.555J
Wikidata:Q81995316
Mol file:50608-12-3.mol

Synonyms:5-tert-Butyl-2-methylamino-1,3,4-thiadiazole

Suppliers and Price of 5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine

Supply Marketing:

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

Total 20 raw suppliers

Chemical Property of 5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine

Chemical Property:

Vapor Pressure:0.0178mmHg at 25°C
Melting Point:80-82 °C
Boiling Point:253.9°C at 760 mmHg
PKA:4.21±0.10(Predicted)
Flash Point:107.4°C
PSA：66.05000
Density:1.13g/cm³
LogP:1.95030
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:171.08301860
Heavy Atom Count:11
Complexity:132

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=NN=C(S1)NC
Uses 5-tert-Butyl-2-methylamino-1,3,4-thiadiazole is used in the synthesis of Tebuthiuron(T013620) which is an nonselective broad spectrum herbicide used to control weeds, woody and herbaceous plants.

Technology Process of 5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine

There total 8 articles about 5-tert-butyl-N-methyl-1,3,4-thiadiazol-2-amine 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: 100.0%

: 50608-12-3
2-tert-butyl-5-methylamino-1,3,4-thiadiazole

Guidance literature:

Reference yield: 98.9%

: 6610-29-3
4-methylthiosemicarbazide

: 75-98-9
Trimethylacetic acid

: 50608-12-3
2-tert-butyl-5-methylamino-1,3,4-thiadiazole

Guidance literature:: Trimethylacetic acid; With phosgene; In toluene; at 80 ℃; for 2h;

4-methylthiosemicarbazide; With triethylamine; In toluene; at 100 ℃; for 3h;