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Merck
CN

12268

Sigma-Aldrich

苯甲亚胺酸乙酯 盐酸盐

≥97.0% (AT)

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About This Item

线性分子式:
C6H5C(=NH)OCH2CH3 · HCl
CAS号:
分子量:
185.65
Beilstein:
3913195
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥97.0% (AT)

mp

~125 °C (dec.)

官能团

ether
phenyl

SMILES字符串

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

一般描述

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

应用

合成中间体

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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.
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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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