Analyzing the synthesis route of 2150-55-2

In some applications, this compound(2150-55-2)Safety of 2-Amino-4,5-dihydrothiazole-4-carboxylic acid is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid(SMILESS: O=C(C1N=C(N)SC1)O,cas:2150-55-2) is researched.Synthetic Route of C8H8N4. The article 《Study on fermentation conditions and culture medium of enzymatic synthesis of L-cysteine》 in relation to this compound, is published in Xiandai Huagong. Let’s take a look at the latest research on this compound (cas:2150-55-2).

L-cysteine synthesizing enzyme could be produced in Pseudomonas sp.TS1138, induced by DL-2-amino-Δ2-thiazoline-4-carboxylic acid (DL-ATC). Optimum conditions suitable for enzyme production in Pseudomonas sp. TS1138 were studied and the results showed that enzymes activity in Pseudomonas sp. TS1138 was highest when the cultivate conditions were as follows: mass concentration of DL-ATC was 5 g/L, glucose and urea were carbon and nitrogen source resp., fermentation temperature was 27-29°C, liquid volume of culture medium was 40 mL in a 500 mL shaking flask. The highest enzymes activity could reach 1,780 U/mL in a 7 L fermentor under the optimum conditions.

In some applications, this compound(2150-55-2)Safety of 2-Amino-4,5-dihydrothiazole-4-carboxylic acid is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem