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Merck

G6600

Sigma-Aldrich

甘氨酸甲酯 盐酸盐

99%, for peptide synthesis

别名:

Glycine methyl ester·HCl, Methyl glycinate hydrochloride

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About This Item

线性分子式:
NH2CH2COOCH3 · HCl
CAS号:
分子量:
125.55
Beilstein:
3593644
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.22

product name

甘氨酸甲酯 盐酸盐, 99%

品質等級

化驗

99%

形狀

powder, crystals or chunks

反應適用性

reaction type: solution phase peptide synthesis

顏色

white

mp

175 °C (dec.) (lit.)

應用

peptide synthesis

SMILES 字串

Cl.COC(=O)CN

InChI

1S/C3H7NO2.ClH/c1-6-3(5)2-4;/h2,4H2,1H3;1H

InChI 密鑰

COQRGFWWJBEXRC-UHFFFAOYSA-N

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一般說明

甘氨酸甲酯盐酸盐又名甲基甘氨酸酯盐酸盐,是一种甘氨酸衍生物,用于制备氨基酸和有机化合物。

應用

甘氨酸甲酯盐酸盐可用于合成以氨基酸酯为侧链的环磷腈类物质。还可在水相中合成多肽,是一种绿色的制肽法。

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

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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Akihiko Tohri et al.
European journal of biochemistry, 271(5), 962-971 (2004-03-11)
To elucidate the domains on the extrinsic 23 kDa protein involved in electrostatic interaction with the extrinsic 33 kDa protein in spinach photosystem II, we modified amino or carboxyl groups of the 23 kDa protein to uncharged methyl ester groups
Wenzhong Gao et al.
Organic letters, 7(19), 4241-4244 (2005-09-09)
[reaction: see text] A novel Cu(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with acrylates has been developed. Up to 98/2 exo/endo selectivity and up to 98% enantiomeric excess have been achieved.
Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.
A Rios et al.
Journal of the American Chemical Society, 123(32), 7949-7950 (2001-08-09)
L P Roguin et al.
The Biochemical journal, 224(2), 535-540 (1984-12-01)
Bovine somatotropin with an increasing number of its carboxylate groups modified by reaction with glycine methyl ester in the presence of a water-soluble carbodi-imide was tested for its activity in different bioassays. Only those derivatives which were known to be
J M Delfino et al.
International journal of peptide and protein research, 21(4), 440-450 (1983-04-01)
The reactivity of the carboxyl groups in bovine growth hormone was studied by reaction with 1-ethyl-3(3-dimethylaminopropyl) carbodiimide in the presence of an excess of glycinemethylester. Localization in the molecule of the various kinetically distinguishable carboxyl groups was achieved. Highest reactivity

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