(4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE

Base Information

• Chemical Name: (4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE
• CAS No.: 75220-48-3
• Molecular Formula: C10H11 Cl N2 S
• Molecular Weight: 226.73
• Hs Code.: 2934100090
• Mol file: 75220-48-3.mol

Synonyms:2-Thiazolamine, N-(4-chlorophenyl)-4,5-dihydro-5-methyl-;N-(4-chlorophenyl)-5-methyl-4,5-dihydro-1,3-thiazol-2-amine

Chemical Property of (4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE

Chemical Property:

• Vapor Pressure: 0.000126mmHg at 25°C
• Boiling Point: 334.7°C at 760 mmHg
• Flash Point: 156.2°C
• PSA: 49.69000
• Density: 1.34g/cm³
• LogP: 2.75180

Purity/Quality:

99% ^*data from raw suppliers

N-(4-Chlorophenyl)-5-methyl-4,5-dihydro-1,3-thiazol-2-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE

There total 1 articles about (4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-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: 63.0%

1-allyl-3-parachlorophenyl-thiourea (14255-79-9) → N-(4-chlorophenyl)-5-methyl-4,5-dihydrothiazol-2-amine (75220-48-3)

Guidance literature:

With hydrogenchloride; In ethanol; Reflux;

DOI:10.1134/S1070363216030312

Reference yield: 85.0%

N-(4-chlorophenyl)-5-methyl-4,5-dihydrothiazol-2-amine (75220-48-3) + dipropyl chlorophosphate (2510-89-6) → {2-[(Z)-4-Chloro-phenylimino]-5-methyl-thiazolidin-3-yl}-phosphonic acid dipropyl ester

Guidance literature:

In benzene;

Reference yield: 71.0%

N-(4-chlorophenyl)-5-methyl-4,5-dihydrothiazol-2-amine (75220-48-3) + O-phenyl methylphosphonochloridothioate (14410-07-2) → {2-[(Z)-4-Chloro-phenylimino]-5-methyl-thiazolidin-3-yl}-methyl-phosphinothioic acid O-phenyl ester

Guidance literature:

In benzene;

upstream raw materials:

1-allyl-3-parachlorophenyl-thiourea

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