Production Method 1

50382-32-6

95453-54-6

Reaction Conditions

1.1 Reagents: Dimethyl sulfoxide ,  Oxalyl chloride Solvents: Dichloromethane ;  -78 °C; 30 min, -78 °C
1.2 Solvents: Dichloromethane ;  -78 °C; 3 h, -78 °C
1.3 Reagents: Triethylamine ;  10 min, -78 °C

Reference

Inhibitors of protein isoprenyl transferases

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Production Method 2

50382-32-6

95453-54-6

Reaction Conditions

1.1 Reagents: Manganese oxide (MnO2) Solvents: Dichloromethane ;  overnight, rt

Reference

Preparation of N-aroyldehydroamino acids as lymphocyte function associated antigen-1 antagonists.

, World Intellectual Property Organization, , ,

Production Method 3

7210-77-7

95453-54-6

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide ,  Diisobutylaluminum hydride Solvents: Tetrahydrofuran ,  Hexane ;  0 - 10 °C; 2 h, rt
1.2 Solvents: Tetrahydrofuran ;  -30 - -20 °C; 4 h, -20 °C
1.3 Reagents: Water

Reference

Preparation of π-electron conjugated fused thiophene derivatives

, Japan, , ,

Production Method 4

95453-54-6

Reaction Conditions

Reference

Preparation process and effect of benzazepine derivatives as CCR5 antagonists

, World Intellectual Property Organization, , ,

2,4-dimethyl-1,3-thiazole-5-carbaldehyde Raw materials

• Ethyl 2,4-dimethylthiazole-5-carboxylate
• (2,4-Dimethyl-1,3-thiazol-5-yl)methanol

2,4-dimethyl-1,3-thiazole-5-carbaldehyde Preparation Products

• 2,4-dimethyl-1,3-thiazole-5-carbaldehyde (95453-54-6)

• 1. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 2. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
  Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
• 3. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 4. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 5. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles 2,4,5-trisubstituted thiazoles
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Thiazoles 2,4,5-trisubstituted thiazoles

• 213258-56-1(2,5-dimethyl-1,3-thiazole-4-carbaldehyde)
• 61292-02-2(5-Thiazolecarboxaldehyde, 4-methyl-2-(3-methylphenyl)-)
• 13623-11-5(2,4,5-Trimethylthiazole)
• 39669-78-8(1,3-Thiazole-4,5-dicarboxaldehyde)
• 38205-60-6(1-(2,4-dimethyl-1,3-thiazol-5-yl)ethan-1-one)
• 53137-27-2(dimethyl-1,3-thiazole-5-carboxylic acid)
• 13669-78-8(Thiazole-4,5-dicarbaldehyde)
• 55327-28-1(5-Thiazolecarboxaldehyde, 4-methyl-2-(4-methylphenyl)-)
• 66806-33-5(dimethyl-1,3-thiazole-5-carboxamide)
• 82294-70-0(4-methyl-1,3-thiazole-5-carbaldehyde)