跳轉至內容
Merck
全部照片(1)

重要文件

690414

Sigma-Aldrich

丙二腈

Arxada quality, ≥99.0% (calculated, GC, KF)

同義詞:

二氰基甲烷

登入查看組織和合約定價


About This Item

線性公式:
CH2(CN)2
CAS號碼:
分子量::
66.06
Beilstein:
773697
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
暫時無法取得訂價和供貨情況

品質等級

化驗

≥99.0% (calculated, GC, KF)

形狀

liquid

品質

Arxada quality

製造商/商標名

Arxada AG

雜質

≤0.10% water
≤0.50% (E)-2-butenedinitrile
≤0.50% (Z)-2-butenedinitrile
≤0.50% butanedinitrile

bp

220 °C (lit.)

mp

30-32 °C (lit.)

密度

1.049 g/mL at 25 °C (lit.)

官能基

nitrile

儲存溫度

2-8°C

SMILES 字串

N#CCC#N

InChI

1S/C3H2N2/c4-2-1-3-5/h1H2

InChI 密鑰

CUONGYYJJVDODC-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

應用

Malononitrile is an active methylene reagent useful for condensation reactions to synthesize various synthetic intermediates and heterocycles.[1][2][3] It is extensively used in the Knoevenagel condensation with various aldehydes and ketones.[1][4]
Some of the reactions where malononitrile is used as a reactant are:
  • Synthesis of 2-pyran-4-ylidene-malononitrile (PM) based red light emitting polymers.[5]
  • Synthesis of polysubstituted dihydropyridines.[6]
  • Synthesis of various chromene derivatives upon treating with salicylic aldehydes.[7]
  • Synthesis of triselenium dicyanide by treating it with selenium dioxide.[8]

象形圖

Skull and crossbonesEnvironment

訊號詞

Danger

危險分類

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

186.8 °F - closed cup

閃點(°C)

86 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

未看到正確版本?

如果您需要一個特定的版本,您可以透過批號來尋找特定憑證。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Malononitrile.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Sun, Jing et al.
Organic Letters, 12(16), 3678-3681 (2010)
Triselenium dicyanide from malononitrile and selenium dioxide. One-pot synthesis of selenocyanates.
Kachanov, Andrey V et al.
Tetrahedron Letters, 45(23), 4461-4463 (2004)
The Knoevenagel condensation reaction of aromatic aldehydes with malononitrile by grinding in the absence of solvents and catalysts.
Ren, Zhongjiao et al.
Synthetic Communications, 32(22), 3475-3479 (2002)
The condensation of salicylaldehydes and malononitrile revisited: synthesis of new dimeric chromene derivatives.
Costa, Marta et al.
The Journal of Organic Chemistry, 73(5), 1954-1962 (2008)

Questions

Reviews

No rating value

Active Filters

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務