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Product introduction
α-甲基-γ-丁内酯发生苄基化反应生成外消旋α-苄基-α-甲基-γ-丁内酯。 以α-甲基-γ-丁内酯为模型化合物,在交叉实验中研究了毛果芸香碱的热力学优势反应位点。 α-Methyl-γ-butyrolactone undergoes benzylation to give racemic α-benzyl-α-methyl-γ-butyrolactone. α-Methyl-γ-butyrolactone was used as model compound in Bracketing experiments to investigate the thermodynamically favored site of reaction of pilocarpine
Chinese name
α-甲基-γ-丁内酯
English name
α-Methyl-γ-butyrolactone
Chinese alias
4,5-二氢-3-甲基-2(3H)-呋喃酮
English alias
4-Hydroxy-2-methylbutyric acid lactone | .alpha.-Methylbutyrolactone | 2(3H)-Furanone, dihydromethyl- | 2-Methyl-laquo gammaRaquo -butyrolactone | 4,5-Dihydro-3-methyl-2(3H)-furanone | 140H0G0P5W | CHEBI:36806 | NSC 102837 | Pavinetant [USAN] | 5-(4,6-Dim
CAS number
1679-47-6
molecular formula
C5H8O2
molecular weight
100.12 g/mol
Exact mass
≥98%(GC)
PSA
26.300 Ų
Logp
0.800
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Research chemical 1g; ≥98%; GC

Research chemical 1g; ≥98%; GC; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1g; ≥98%; GC.

item number:A151225-1g
Product model:1g
level: 1g; ≥98%; GC
Lead Time:30days
sold 81 Items
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1g

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