5-(1-Ethylpropyl)-1,3,4-thiadiazol-2-amine

Base Information

• Chemical Name: 5-(1-Ethylpropyl)-1,3,4-thiadiazol-2-amine
• CAS No.: 229003-14-9
• Molecular Formula: C7H13N3S
• Molecular Weight: 171.266
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID20352730
• Wikidata: Q82130030
• ChEMBL ID: CHEMBL4588890
• Mol file: 229003-14-9.mol

Synonyms:229003-14-9;5-(1-ethylpropyl)-1,3,4-thiadiazol-2-amine;5-(pentan-3-yl)-1,3,4-thiadiazol-2-amine;5-pentan-3-yl-1,3,4-thiadiazol-2-amine;Enamine_005414;SCHEMBL3897457;CHEMBL4588890;DTXSID20352730;HMS1409G02;BBL007651;MFCD01131203;STK500410;AKOS001054009;LS-03068;CS-0044689;EN300-05646;Z56907638

Chemical Property of 5-(1-Ethylpropyl)-1,3,4-thiadiazol-2-amine

Chemical Property:

• PSA: 80.04000
• LogP: 2.60510
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 171.08301860
• Heavy Atom Count: 11
• Complexity: 116

Purity/Quality:

98%+ ^*data from raw suppliers

5-(1-Ethylpropyl)-1,3,4-thiadiazol-2-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(CC)C1=NN=C(S1)N

Technology Process of 5-(1-Ethylpropyl)-1,3,4-thiadiazol-2-amine

There total 2 articles about 5-(1-Ethylpropyl)-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: 51.0%

2-Ethylbutanoic acid (88-09-5) + thiosemicarbazide (79-19-6) → 5-(pentan-3-yl)-1,3,4-thiadiazol-2-amine (229003-14-9)

Guidance literature:

With sulfuric acid; at 85 ℃; for 7h;

Reference yield:

chlorure d'acide ethyl-2 butyrique (2736-40-5) + thiosemicarbazide (79-19-6) → 5-(pentan-3-yl)-1,3,4-thiadiazol-2-amine (229003-14-9)

Guidance literature:

Reference yield: 72.0%

5-(pentan-3-yl)-1,3,4-thiadiazol-2-amine (229003-14-9) + 2-nitro-4,5-diethoxybenzoic acid (103796-34-5) → 4,5-diethoxy-2-nitro-N-(5-(pentan-3-yl)-1,3,4-thiadiazol-2-yl)benzamide

Guidance literature:

2-nitro-4,5-diethoxybenzoic acid; With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; for 0.166667h;

5-(pentan-3-yl)-1,3,4-thiadiazol-2-amine; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1016/j.chembiol.2017.12.011

upstream raw materials:

chlorure d'acide ethyl-2 butyrique

thiosemicarbazide

2-Ethylbutanoic acid

Downstream raw materials:

sulfanilic acid-[5-(1-ethyl-propyl)-[1,3,4]thiadiazol-2-ylamide]

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