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About This Item
线性分子式:
(CH3)2CHCH2COCO2Na · xH2O
CAS号:
分子量:
152.12 (anhydrous basis)
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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方案
≥98%
表单
solid
mp
280 °C (dec.) (lit.)
SMILES字符串
O.[Na+].CC(C)CC(=O)C([O-])=O
InChI
1S/C6H10O3.Na.H2O/c1-4(2)3-5(7)6(8)9;;/h4H,3H2,1-2H3,(H,8,9);;1H2/q;+1;/p-1
InChI key
FUDIEMDWYRETTC-UHFFFAOYSA-M
应用
Condensation with α-amino ketones and subsequent cyclization provides pyrazinones.
替代产品
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Heterocycles, 31, 1647-1647 (1990)
D A Roberts et al.
Journal of medicinal chemistry, 33(9), 2326-2334 (1990-09-01)
A series of 1,2,4-triazolo[4,3-a]pyrazine derivatives with human renin inhibitory activity, which incorporate (1S,2S)-2-amino-1,3-dicyclohexyl-1-hydroxypropane, statine (Sta), and (3S,4S)-4-amino-5-cyclohexyl-3-hydroxy-pentanoic acid (ACHPA) transition-state mimetics, have been prepared. Structure-activity relationships for renin inhibitory activity in the series are consistent with the 2-[8-isobutyl-6-phenyl-1,2,4-triazolo[4,3-a]pyrazin-3-yl]-3-(3 pyridyl)propionic acid
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