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phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside

Base Information Edit
  • Chemical Name:phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside
  • CAS No.:132351-74-7
  • Molecular Formula:C19H30O3Si
  • Molecular Weight:334.531
  • Hs Code.:
  • Mol file:132351-74-7.mol
phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside

Synonyms:phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside

Suppliers and Price of phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside Edit
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Technology Process of phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside

There total 9 articles about phenylmethyl 2,3,6-trideoxy-4-O-<(1,1-dimethylethyl)dimethylsilyl>-α-L-erythro-hex-2-enopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: NaOMe / methanol
2: 91 percent / imidazole / CH2Cl2
With 1H-imidazole; sodium methylate; In methanol; dichloromethane;
DOI:10.1021/jo951560x
Guidance literature:
Multi-step reaction with 3 steps
1: BF3*Et2O / CH2Cl2
2: NaOMe / methanol
3: 91 percent / imidazole / CH2Cl2
With 1H-imidazole; boron trifluoride diethyl etherate; sodium methylate; In methanol; dichloromethane;
DOI:10.1021/jo951560x
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