CAS 26595-78-8 2-amino-N-ethylacetamide hydrochloride (HCID 21257306)

基本情報

CAS: 26595-78-8
標準SMILES: CCNC(=O)CN.Cl
InChIKey: RSNDLRFBYCPDDU-UHFFFAOYSA-N
分子式: C4H11ClN2O
平均分子量: 138.59 g/mol
単同位体質量: 138.0559907

名称と識別子

優先名称: 2-amino-N-ethylacetamide hydrochloride
IUPAC: 2-amino-N-ethylacetamide;hydrochloride
現地名: 2-アミノ-N-エチルアセトアミド塩酸塩
英語名: 2-AMINO-N-ETHYL-ACETAMIDE HYDROCHLORIDE
分子式: C4H11ClN2O
分子量: 138.6

名称と別名

2-AMINO-N-ETHYLACETAMIDE HYDROCHLORIDERefChem:465040816-809-426595-78-8MFCD08060119Acetamide, 2-amino-N-ethyl-, hydrochloride (1:1)Glycine N-Ethyl Amide Hydrochloride2-amino-N-ethylacetamide;hydrochloride2-AMINO-N-ETHYLACETAMIDE HCL2-AMINO-N-ETHYL-ACETAMIDE HYDROCHLORIDE2-Amino-N-ethyl-Acetamide HClAcetamide, 2-amino-N-ethyl-, monohydrochloride

名称をさらに表示

2-アミノ-N-エチルアセトアミド塩酸塩

Glycine N-Ethyl Amide HClN-ethylglycinamide HCl saltGlycine ethylamide hydrochlorideSCHEMBL3649029DTXSID10611702RSNDLRFBYCPDDU-UHFFFAOYSA-NBBA59578AKOS015847715

データベース識別子

CAS: 26595-78-8
PubChem CID: 21257306
DTXSID: DTXSID10611702
EC Number: 816-809-4

物性

構造計算による物性

極性表面積: 55.1 Å²
水素結合供与体数: 3
水素結合受容体数: 2
回転可能結合数: 2
重原子数: 8
形式電荷: 0
複雑度: 62

物理化学的性質

貯蔵温度: Inert atmosphere,Room Temperature

安全と法規制

GHS分類

GHS Classification · 5 件

Warning

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]；H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]；H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

危険有害性情報

Hazard Classes and CategoriesSkin Irrit. 2 (100%)；Eye Irrit. 2A (100%)；STOT SE 3 (100%)

安全データ

hazard_class: IRRITANT

化学と産業

応用分野 · 1 件

使用Glycine N-Ethyl Amide Hydrochloride is a derivative of Glycine (G615990) and is used as a reagent in the synthesis of quinoxaline derivatives as antivirus agents. Also used as a reagent in the synthesis of phenylpiperidine derivatives as peripheral opioid antagonists.

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化合物ノート

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