21057
Calcium borohydride bis-tetrahydrofuran complex
≥98.0%
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Assay
≥98.0%
reaction suitability
reagent type: reductant
SMILES string
[BH4-].[BH4-].[Ca++].C1CCOC1.C2CCOC2
Other Notes
Ready-to-use, selective reducing agent; e.g. mild reduction of esters
Regulatory Information
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Synthesis, 459-459 (1990)
Heterocycles, 7, 1027-1027 (1977)
Journal of medicinal chemistry, 33(7), 1898-1905 (1990-07-01)
As an extension of the previous investigation (J. Med. Chem. 1988, 31, 919), we synthesized a series of 2-[2-[(aminoalkyl)oxy]-5-methoxyphenyl]-3,4-dihydro-4-methyl-3-oxo-2H- 1,4-benzothiazines (3) and evaluated their Ca2+ antagonistic activities. Ca2+ antagonistic activity was measured with isolated depolarized guinea pig taenia cecum. On
Tetrahedron, 45, 5051-5051 (1989)
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