12268
Ethyl benzimidate hydrochloride
≥97.0% (AT)
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About This Item
Fórmula linear:
C6H5C(=NH)OCH2CH3 · HCl
Número CAS:
Peso molecular:
185.65
Beilstein:
3913195
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
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Nível de qualidade
Ensaio
≥97.0% (AT)
pf
~125 °C (dec.)
grupo funcional
ether
phenyl
cadeia de caracteres SMILES
Cl[H].CCOC(=N)c1ccccc1
InChI
1S/C9H11NO.ClH/c1-2-11-9(10)8-6-4-3-5-7-8;/h3-7,10H,2H2,1H3;1H
chave InChI
MODZVIMSNXSQIH-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Ethyl benzimidate hydrochloride reacts with (R)-ethyl cysteine hydrochloride in ethanol to yield (4R)-ethyl 2-phenyl-4,5-dihydrothiazole-4-carboxylate. It reacts with D-Penicillamine methyl ester hydrochloride and triethylamine to yield methyl-5,5- dimethyl-2-phenyl-2-thiazoline-4-carboxylate.
Aplicação
Intermediate for synthesis
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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
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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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