产品名称
Riboflavin, 2′,3′,4′,5′-tetraacetate, >95%
InChI
InChI=1S/C25H28N4O10/c1-11-7-17-18(8-12(11)2)29(23-21(26-17)24(34)28-25(35)27-23)9-19(37-14(4)31)22(39-16(6)33)20(38-15(5)32)10-36-13(3)30/h7-8,19-20,22H,9-10H2,1-6H3,(H,28,34,35)/t19-,20+,22-/m0/s1
InChI key
VKVDYPHLGLIXAG-VWPQPMDRSA-N
SMILES string
O=C(N1)C2=NC3=CC(C)=C(C)C=C3N(C[C@H](OC(C)=O)[C@@H]([C@H](OC(C)=O)COC(C)=O)OC(C)=O)C2=NC1=O
assay
>95%
form
powder or crystals, solid
reaction suitability
reagent type: catalyst
reaction type: Photocatalysis
storage condition
dry at room temperature, protect from light
color
light yellow to dark yellow
Quality Level
General description
Riboflavin, 2′,3′,4′,5′-tetraacetate is the acetate-protected derivative of riboflavin (vitamin B2) a vitamin found in food and used as a dietary supplement.
Application
Riboflavin, 2′,3′,4′,5′-tetraacetate has been used as a photocatalyst for the ring-opening of cyclic amines.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
David M Soro et al.
Journal of the American Chemical Society, 145(20), 11245-11257 (2023-05-12)
Described herein are studies toward the core modification of cyclic aliphatic amines using either a riboflavin/photo-irradiation approach or Cu(I) and Ag(I) to mediate the process. Structural remodeling of cyclic amines is explored through oxidative C-N and C-C bond cleavage using
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