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线性分子式:
C6H5C(=NH)OCH2CH3 · HCl
化学文摘社编号:
分子量:
185.65
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-248-1
Beilstein/REAXYS Number:
3913195
MDL number:
产品名称
苯甲亚胺酸乙酯 盐酸盐, ≥97.0% (AT)
InChI key
MODZVIMSNXSQIH-UHFFFAOYSA-N
InChI
1S/C9H11NO.ClH/c1-2-11-9(10)8-6-4-3-5-7-8;/h3-7,10H,2H2,1H3;1H
SMILES string
Cl[H].CCOC(=N)c1ccccc1
assay
≥97.0% (AT)
mp
~125 °C (dec.)
functional group
ether
phenyl
Quality Level
Application
合成中间体
General description
盐酸苯丙二酸乙酯与(R)-乙基半胱氨酸盐酸盐在乙醇中反应,生成(4R)-2-苯基-4,5-二氢噻唑-4-羧酸乙酯。它与 D-青霉胺甲酯盐酸盐和三乙胺反应,生成 5,5-二甲基-2-苯基-2-噻唑啉-4-羧酸甲酯。
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
法规信息
新产品
此项目有
The Synthesis of Substituted Penicillins and Simpler Structural Analogs. III. Phthalimido ?-Lactam-Thiazolidines Derived from Penicillamine.
Sheehan JC, et al.
Journal of the American Chemical Society, 73(9), 4373-4375 (1951)
Satendra Singh et al.
The Journal of organic chemistry, 69(13), 4551-4554 (2004-06-19)
(1R)-(+)-2,10- and (1S)-(-)-2,10-camphorsultam were acylated with ethyl 2-phenylthiazoline 4-carboxylate to afford (+)- and (-)-2-phenylthiazolinylcamphorsultam, which were stereoselectively alkylated with MeI in the presence of n-BuLi. Alkylation of these phenylthiazolinylcamphorsultams occurred from the beta-face rather than alpha-face, resulting in the formation
Aerobic dissipation of the novel cyanoacrylate fungicide phenamacril in soil and sludge incubations.
Søren S Donau et al.
Chemosphere, 233, 873-878 (2019-07-26)
The cyanoacrylate ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate (phenamacril), has been introduced as an effective agent against several fungi species belonging to the Fusarium genus. However, in current literature, knowledge about the environmental behavior of this fungicide is limited and there are no data
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