Analyzing the synthesis route of 2150-55-2

After consulting a lot of data, we found that this compound(2150-55-2)Recommanded Product: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid can be used in many types of reactions. And in most cases, this compound has more advantages.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Enzymatic production of L-cysteine from DL-2-amino-Δ2-thiazoline-4-carboxylic acid by Pseudomonas thiazolinophilum: optimal conditions for the enzyme formation and enzymatic reaction, published in 1978-12-31, which mentions a compound: 2150-55-2, mainly applied to Pseudomonas enzyme cysteine, Recommanded Product: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid.

Cultivation of P. thiazolinophilum AJ 3854 for the production of the enzyme which could form L-cysteine [52-90-4] from DL-2-amino-Δ2-thiazoline-4-carboxylic acid (I) [2150-55-2] and the reaction conditions of this enzyme were investigated. This enzyme was inducible, intracellular, and growth-associated A marked inactivation of enzyme was observed, especially in the growing phase, but could be prevented by 1∼10 mM Mn2+ or by I as inducer at the mid-logarithmic phase. Enzymic degradation of L-cysteine (or L-cystine [56-89-3]) formed from I could be prevented by the addition of hydroxylamine or semicarbazide. Thus, L-cysteine and L-cystine were quant. produced from I. Optimal pH and temperature of enzymic reaction were 8.2 and 42° (2 h), resp. A sigmoidal reaction curve was observed when intact cells were used as enzyme source, but sonic treatment of cells made the curve linear.

After consulting a lot of data, we found that this compound(2150-55-2)Recommanded Product: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem