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Merck
CN

C88505

氰乙酸

99%

别名:

2-氰基乙酸, 单氰基乙酸, 氰基乙酸

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线性分子式:
NCCH2COOH
化学文摘社编号:
分子量:
85.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-743-9
Beilstein/REAXYS Number:
506325
MDL number:
Assay:
99%
Form:
crystals
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InChI key

MLIREBYILWEBDM-UHFFFAOYSA-N

InChI

1S/C3H3NO2/c4-2-1-3(5)6/h1H2,(H,5,6)

SMILES string

OC(=O)CC#N

vapor pressure

0.1 mmHg ( 100 °C)

assay

99%

form

crystals

bp

108 °C/0.15 mmHg (lit.)

mp

64-70 °C (lit.)

solubility

H2O: 50 mg/mL, clear, colorless to very faintly yellow

Quality Level

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Application

氰基乙酸可用作以下反应的试剂:
  • 与乙酸酐一起用于各种吡咯、吲哚和苯胺衍生物的氰基乙酰化(cyanoacetylation)。它也可用于环化、香豆素和其他杂环的合成等其他反应中
  • 。通过Knoevenagel缩合反应制备可作为MT3受体配体的5-乙酰氨基取代褪黑素衍生物的全合成过程的关键中间体。
  • 通过Ugi加成物与氰基乙酸和芳香醛反应合成氨基吡咯啉酮(aminopyrrolinone )衍生物。

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

supp_hazards

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Cyanoacetylation of indoles, pyrroles and aromatic amines with the combination cyanoacetic acid and acetic anhydride
Slaett J, et al.
Synthesis, 2004(16), 2760-2765 (2004)
The Ugi Reaction of Cyanoacetic Acid as a Route to Tetramic Acid Derivatives
Alvarez-Rodriguez NV, et al.
Synlett, 26(16), 2253-2256 (2015)
Synthesis of novel ??3 receptor ligands via an unusual Knoevenagel condensation
Volkova MS, et al.
Bioorganic & medicinal chemistry letters, 22(24), 7578-7581 (2012)
Kan Wang et al.
Chemical biology & drug design, 75(3), 277-283 (2010-07-28)
The design of an unprecedented multicomponent reaction to and synthesis of 2-amino-5-ketoaryl pyrroles are described. The compounds (14 examples) can be synthesized by reacting aminoacetophenone sulfonamides, (hetero)aromatic aldehydes, and malonodinitrile or cyanoacetic acid derivatives in one-pot manner. Pharmacophore features and
Julien Warnan et al.
Macromolecular rapid communications, 32(15), 1190-1194 (2011-06-29)
A series of three poly(3-hexylthiophene) functionalized either with a cyanoacetic acid (CA) or a rhodanine-3-acetic acid anchoring groups were synthesized and characterized. The TiO(2) based dye-sensitized solar cells have been fabricated and performances were tested. We show that shorter chain

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