321371-28-2

Basic information

• Product Name: Methyl 2-dichloroMethyl-4,5-dihydrothiazole-4-carboxylate
• Synonyms: Methyl 2-dichloroMethyl-4,5-dihydrothiazole-4-carboxylate
• CAS NO: 321371-28-2
• Molecular Formula: C6H7Cl2NO2S
• Molecular Weight: 228.09628
• Mol File: 321371-28-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 264.8±40.0 °C(Predicted)
• Appearance: /
• Density: 1.61±0.1 g/cm3(Predicted)
• PKA: 0.40±0.40(Predicted)
• CAS DataBase Reference: Methyl 2-dichloroMethyl-4,5-dihydrothiazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-dichloroMethyl-4,5-dihydrothiazole-4-carboxylate(321371-28-2)
• EPA Substance Registry System: Methyl 2-dichloroMethyl-4,5-dihydrothiazole-4-carboxylate(321371-28-2)

Safety Data

• Hazardous Substances Data: 321371-28-2(Hazardous Substances Data)

Upstream product

• 3018-12-0 dichloroacetonitrile 
• 5714-80-7 cysteine methyl ester hydrochloride 
• 18598-63-5 L-cysteine methyl ester hydrochloride 

Downstream Products

• 321371-29-3 2-chloromethyl-1,3-thiazole-4-carboxylic acid methyl ester 

Relevant articles and documents

Incorporation of heterocycles into the backbone of peptoids to generate diverse peptoid-inspired one bead one compound libraries

Combinatorial libraries of peptoids (oligo-N-substituted glycines) have proven to be useful sources of protein ligands. Each unit of the peptoid oligomer is derived from 2-haloacetic acid and a primary amine. To increase the chemical diversity available in peptoid libraries, we demonstrate here that heterocyclic halomethyl carboxylic acids can be employed as backbone building blocks in the synthesis of peptoid-based oligomers. Optimized conditions are reported that allow the creation of large, high quality combinatorial libraries containing these units.