推荐产品
品質等級
化驗
94%
形狀
liquid
雜質
4-5% dimethyl dichloromalonate
折射率
n20/D 1.437 (lit.)
bp
105-106 °C/19 mmHg (lit.)
密度
1.305 g/mL at 25 °C (lit.)
官能基
chloro
ester
SMILES 字串
COC(=O)C(Cl)C(=O)OC
InChI
1S/C5H7ClO4/c1-9-4(7)3(6)5(8)10-2/h3H,1-2H3
InChI 密鑰
LNBQBURECUEBKZ-UHFFFAOYSA-N
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一般說明
Dimethyl chloromalonate (dimethyl 2-chloromalonate) is a dialkyl 2-substituted malonate. Carbanions of dimethyl chloromalonate are reported to react with naphthoquinone derivatives, via vicarious nucleophilic substitution or oxidative nucleophilic substitution of hydrogen processes. Dimethyl chloromalonate is reported to react with hydroquinone and monosubstituted hydroquinones to afford 2-oxido-benzo[b]furan derivatives. Synthesis of dimethyl 2-chloromalonate, via chlorination of dimethyl malonate has been reported.
應用
Dimethyl chloromalonate is suitable for use in the synthesis of 4,5,6-trichloropyrimidine. It may be used in the stereoselective synthesis of highly functionalized nitrocyclopropanes. It may be used in one-pot synthesis of tetra-alkoxycarbonylallylidenetriphenylphosphoranes.
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
224.6 °F - closed cup
閃點(°C)
107 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
其他客户在看
A preparative method for Synthesis of 4, 5, 6-trichloropyrimidine.
ARKIVOC (Gainesville, FL, United States), 6, 905-908 (2000)
The Journal of organic chemistry, 71(19), 7494-7497 (2006-09-09)
A convenient and novel one-pot organocatalytic methodology for the stereoselective synthesis of highly functionalized nitrocyclopropanes is reported. The addition of dimethyl chloromalonate to a variety of nitroolefins catalyzed by tertiary amines leads to a Michael adduct which cyclizes to form
The reaction of hydroquinone and monosubstituted hydroquinones with dimethyl chloromalonate.
Journal of the Chemical Society. Perkin Transactions 1, 2382-2386 (1979)
An Efficient and Practical Synthesis of Dimethyl 2-chloromalonate.
Der Pharma Chemica, 3(6) (2011)
New one-pot synthesis of tetra-alkoxycarbonylallylidenetriphenylphosphoranes.
Tetrahedron Letters, 39(9), 1051-1054 (1998)
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