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M51008

Sigma-Aldrich

甲基亚氨二乙酸

99%

同義詞:

MIDA, MIDA 配体

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About This Item

線性公式:
CH3N(CH2CO2H)2
CAS號碼:
4408-64-4
分子量：:
147.13
EC號碼:
224-557-6
MDL號碼:
MFCD00004284
分類程式碼代碼:
12352100
PubChem物質ID:
24896977
NACRES:
NA.22

化驗

99%

mp

220 °C (dec.) (lit.)

SMILES 字串

CN(CC(O)=O)CC(O)=O

InChI

1S/C5H9NO4/c1-6(2-4(7)8)3-5(9)10/h2-3H2,1H3,(H,7,8)(H,9,10)

InChI 密鑰

XWSGEVNYFYKXCP-UHFFFAOYSA-N

相關類別

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

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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分析證明 (COA)

Lot/Batch Number
SHBM0764
SHBL9171
SHBL0872
SHBH1876V
SHBF6763V

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Gas-liquid chromatography and enzymatic determination of alanopine and strombine in tissues of marine invertebrates.
K B Storey et al.
Analytical biochemistry, 125(1), 50-58 (1982-09-01)
Alanopine and strombine are novel imino acids produced by a dehydrogenase found in the adductor muscle of the oyster, Crassostrea gigas.
J H Fields et al.
Archives of biochemistry and biophysics, 201(1), 110-114 (1980-04-15)
M Sato et al.
Analytical biochemistry, 174(2), 623-627 (1988-11-01)
A new method for the quantitative analysis of acidic opines--alanopine, strombine, tauropine, and beta-alanopine--is presented. The method is based on formation of phenylthiocarbamyl (PTC) derivatives of the acidic opines after partial purification by ion-exchange chromatography. The PTC acidic opines are
Wan-Yu Deng et al.
IEEE transactions on neural networks and learning systems, 30(4), 1180-1190 (2018-09-04)
In most domain adaption approaches, all features are used for domain adaption. However, often, not every feature is beneficial for domain adaption. In such cases, incorrectly involving all features might cause the performance to degrade. In other words, to make
Mengping Guo et al.
Organic & biomolecular chemistry, 12(36), 7136-7139 (2014-08-12)
N-Methyliminodiacetic acid (MIDA) as a simple, air stable and water-soluble ligand has been used in the palladium-catalyzed Hiyama cross-coupling reaction of trimethoxyphenylsilane with aryl halides. The yield of the corresponding Hiyama coupling products is high up to around 90% in
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Suzuki Miyaura Cross Coupling

The Suzuki-Miyaura cross-coupling reaction is one of the most important and highly utilized reactions in organic chemistry, with applications in polymer science as well as in the fine chemicals and pharmaceutical industries.

Suzuki Miyaura Cross Coupling

The Suzuki-Miyaura cross-coupling reaction is one of the most important and highly utilized reactions in organic chemistry, with applications in polymer science as well as in the fine chemicals and pharmaceutical industries.

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