42604
甘氨酸叔丁酯 盐酸盐
puriss., ≥99.0% (AT)
别名:
叔丁基氨基乙酸酯 盐酸盐
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
H2NCH2CO2C(CH3)3 · HCl
化学文摘社编号:
分子量:
167.63
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
3989048
产品名称
甘氨酸叔丁酯 盐酸盐, puriss., ≥99.0% (AT)
InChI key
OSWULUXZFOQIRU-UHFFFAOYSA-N
InChI
1S/C6H13NO2.ClH/c1-6(2,3)9-5(8)4-7;/h4,7H2,1-3H3;1H
SMILES string
Cl.CC(C)(C)OC(=O)CN
grade
puriss.
assay
≥99.0% (AT)
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
141-143 °C (lit.)
solubility
H2O: 0.1 g/mL, clear, colorless
application(s)
peptide synthesis
Quality Level
正在寻找类似产品? 访问 产品对比指南
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Baptiste Thierry et al.
Molecular diversity, 9(4), 277-290 (2005-11-29)
Cross-linked polystyrene-bound and poly(ethylene glycol)-bound phase-transfer catalysts as well as homopolymers of cinchona alkaloid derivatives have been synthesised. Both soluble and insoluble polymers have been investigated. The enantioselective alkylation of N-diphenyl methylene glycine t-butyl ester has been successfully carried out
S Sarhan et al.
Arzneimittel-Forschung, 34(6), 687-690 (1984-01-01)
The synergistic amplification of the anticonvulsant effects of direct and indirect GABA agonists by glycine has previously been demonstrated. We show in the present report that the anticonvulsant effect of vinyl GABA, a GABA-T (4-aminobutyrate: 2-oxoglutarate aminotransferase) inhibitor with antiepileptic
M Nakoji et al.
Organic letters, 3(21), 3329-3331 (2001-10-12)
[reaction: see text]. A chiral phase-transfer catalyst has been applied to the asymmetric allylation of the tert-butyl glycinate-benzophenone Schiff base with various allylic acetates for the first time to give the allylated products in good yields and with comparable to
Ming-Qing Hua et al.
Chemical communications (Cambridge, England), 47(5), 1631-1633 (2010-12-01)
An efficient, catalytic, diastereo- and enantioselective conjugate addition of N-(diphenylmethylene)glycine tert-butyl ester to β-aryl substituted enones was realized in the presence of 1 mol% of newly desired dinuclear N-spiro-ammonium salts, affording functionalized α-amino acid derivatives in 57-98% yields with high
V De Filippis et al.
Biochemistry, 37(39), 13507-13515 (1998-09-30)
Hirudin is the most potent and specific inhibitor of thrombin, a key enzyme in the coagulation process existing in equilibrium between its procoagulant (fast) and anticoagulant (slow) form. In a previous study, we described the solid-phase synthesis of a Trp3
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持