280143
2-甲氧氨基-2-(2-氨基噻唑)-4-乙酸，主要为顺式
97%
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关于此项目
经验公式（希尔记法）:
C6H7N3O3S
化学文摘社编号:
分子量:
201.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
265-957-0
MDL number:
产品名称
2-甲氧氨基-2-(2-氨基噻唑)-4-乙酸，主要为顺式, 97%
Quality Level
InChI key
NLARCUDOUOQRPB-RUDMXATFSA-N
InChI
1S/C6H7N3O3S/c1-12-9-4(5(10)11)3-2-13-6(7)8-3/h2H,1H3,(H2,7,8)(H,10,11)/b9-4+
SMILES string
CO\N=C(\C(O)=O)c1csc(N)n1
assay
97%
mp
192 °C (dec.) (lit.)
functional group
carboxylic acid
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Total Synthesis of Sodium (3S, 4R)-3-[2-(2-Aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-4-methoxymethyl-2-azetidinone-1-sulfonate from D-Aspartic Acid.
Chung BY, et al.
Bull. Korean Chem. Soc., 13(3), 315-316 (1992)
Total Synthesis of Sodium (3R, 4S)-3-(2-(2-Aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido)-4-methoxymethyl-2-azetidinone-1-sulfonate from L-Aspartic Acid.
Chung BY, et al.
Bull. Korean Chem. Soc., 13(3), 311-314 (1992)
J V Uri et al.
Acta microbiologica Hungarica, 39(3-4), 317-322 (1992-01-01)
Diazald, a chemical intermediate for the synthesis of biologically active compounds, was found to be a potent in vitro antimicrobial agent against yeasts, yeast-like and filamentous fungi as well as Gram-positive and Gram-negative bacterial strains. Its activity is not inhibited
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