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Merck

226319

Sigma-Aldrich

异氰基乙酸乙酯

95%

别名:

α-异氰基乙酸乙酯, α异氰基乙酸乙酯, (乙氧基羰基)异氰甲烷, 2-乙氧基-2-氧代乙基异氰化物, 2-乙氧基羰甲基异氰化物, 2-异氰基乙酸乙酯, 乙氧基羰甲基异氰化物, 异氰基乙酸乙酯

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About This Item

线性分子式:
CNCH2COOCH2CH3
CAS号:
分子量:
113.11
Beilstein:
3588613
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

95%

形狀

liquid

折射率

n20/D 1.418 (lit.)

bp

194-196 °C (lit.)

密度

1.035 g/mL at 25 °C (lit.)

官能基

amine

儲存溫度

2-8°C

SMILES 字串

CCOC(=O)C[N+]#[C-]

InChI

1S/C5H7NO2/c1-3-8-5(7)4-6-2/h3-4H2,1H3

InChI 密鑰

FPULFENIJDPZBX-UHFFFAOYSA-N

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一般說明

异氰酸乙酯是一种异氰酸酯,是生产杂环的合成砌块。

應用

异氰基乙酸乙酯被用于合成7-氮杂-四氢吲哚。它还被用于制备吡咯、噁唑啉、苯二氮卓类、噁唑和咪唑

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

183.2 °F - closed cup

閃點(°C)

84 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Marcus Baumann et al.
Organic letters, 8(23), 5231-5234 (2006-11-03)
[Structure: see text] A multipurpose mesofluidic flow reactor capable of producing gram quantities of material has been developed as an automated synthesis platform for the rapid on-demand synthesis of key building blocks and small exploratory libraries. The reactor is configured
Yifei Li et al.
Chemical communications (Cambridge, England), 48(100), 12228-12230 (2012-11-13)
A novel and efficient route for the synthesis of 7-aza-tetrahydroindoles from N-aryl/alkyl-alkenoylacetamides and ethyl isocyanoacetate is described. A mechanism, involving a stepwise [3+2] cycloaddition-intramolecular aza-Michael addition cascade, is proposed that explains the origin of the double nucleophilic attack on the
Chikashi Kanazawa et al.
Journal of the American Chemical Society, 128(33), 10662-10663 (2006-08-17)
The copper-catalyzed reaction between two different isocyanides produces the corresponding heteroaromatization products, imidazoles, in good yields. The reaction proceeds most probably through the activation of the sp3 C-H bond in the isocyanides by a copper catalyst, followed by a [3
Z Q Gu et al.
Journal of medicinal chemistry, 36(8), 1001-1006 (1993-04-16)
A series of imidazo[1,5-a][1,4]benzodiazepine esters have been synthesized with varying ester side chains and 8-position substituents. The affinities of these compounds were evaluated at both "diazepam-insensitive" (DI) and diazepam-sensitive (DS) subtypes of the benzodiazepine receptor (BZR). A profound steric effect
Tetrahedron Letters, 47, 5481-5481 (2006)

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