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Merck

391549

Sigma-Aldrich

氨基丙二酸二乙酯 盐酸盐

97%

别名:

Aminomalonic acid dimethyl ester 盐酸盐

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About This Item

线性分子式:
NH2CH(COOCH3)2 · HCl
CAS号:
分子量:
183.59
Beilstein:
3696467
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

crystals

mp

160 °C (dec.) (lit.)

溶解度

water: soluble 25 mg/mL, clear, colorless to faintly yellow

SMILES 字串

Cl[H].COC(=O)C(N)C(=O)OC

InChI

1S/C5H9NO4.ClH/c1-9-4(7)3(6)5(8)10-2;/h3H,6H2,1-2H3;1H

InChI 密鑰

QWNDKNJSEWOEDM-UHFFFAOYSA-N

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一般說明

Dimethyl aminomalonate hydrochloride is a hydrochloride salt of a dialkyl aminomalonate.

應用

Dimethyl aminomalonate hydrochloride (aminomalonic acid dimethyl ester hydrochloride) may be used in synthesis of methyl 3-phenyl-5-hydantoincarboxylate and Boc-Leu-Ama(OMe)2(Boc= tert-butyloxycarbonyl, Leu= leucine, Ama= aminomalonic acid). It may be used as starting reagent in the synthesis of the following:
  • (R,S)-2-phenethylcysteine hydrochloride
  • dimethyl 2,2,2-polynitroalkylnitroaminonitromalonate
  • spirotryprostatin B

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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其他客户在看

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Synthesis of Nitro Compounds Starting with Dialkyl Aminomalonates.
Ishchenko MA, et al.
Russ. J. Org. Chem., 37(2), 194-197 (2001)
D Krumme et al.
FEBS letters, 436(2), 209-212 (1998-10-22)
Novel peptides containing the sequence -Pro-Leu-Ama(NHOH)- were synthesized and characterized by spectroscopic techniques. Their inhibitory properties towards the activated form of native human gelatinase B (MMP-9) and the catalytic domain of neutrophil collagenase (cdMMP-8) were determined. The most effective inhibitor
Alpha-alkylcysteines as inhibitors for carboxypeptidase A. Synthesis, evaluation, and implication for inhibitor design strategy.
Lee HS and Kim DH.
Bull. Korean Chem. Soc., 23(4), 593-598 (2002)
Heterocyclizations, XIV. 1,3,5,7,-Tetraoxoperhydroimidazo[1,5-c]imidazole, a Novel Bridgehead Nitrogen Ureide
Capuano L, et al.
Chemische Berichte, 107(10), 3237-3245 (1974)
Oxindole as starting material in organic synthesis.
Ziarani GM, et al.
ARKIVOC (Gainesville, FL, United States), 1, 470-535 (2013)

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