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Merck
모든 사진(1)

주요 문서

12268

Sigma-Aldrich

Ethyl benzimidate hydrochloride

≥97.0% (AT)

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About This Item

Linear Formula:
C6H5C(=NH)OCH2CH3 · HCl
CAS Number:
Molecular Weight:
185.65
Beilstein:
3913195
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥97.0% (AT)

mp

~125 °C (dec.)

작용기

ether
phenyl

SMILES string

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

InChI key

MODZVIMSNXSQIH-UHFFFAOYSA-N

일반 설명

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.

애플리케이션

Intermediate for synthesis

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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
Søren S Donau et al.
Chemosphere, 233, 873-878 (2019-07-26)
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