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| (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane Basic information |
Product Name: | (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane | Synonyms: | (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane;glucocochlearin(1-);β-D-Glucopyranose, 1-thio-, 1-[2-methyl-N-(sulfooxy)butanimidate] | CAS: | 499-24-1 | MF: | C11H21NO9S2 | MW: | 375.41 | EINECS: | | Product Categories: | | Mol File: | 499-24-1.mol | |
| (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane Chemical Properties |
density | 1.71±0.1 g/cm3(Predicted) | pka | -2.94±0.18(Predicted) |
| (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane Usage And Synthesis |
Definition | ChEBI: An alkylglucosinolate that is the conjugate base of glucocochlearin. |
| (2S,3R,4S,5R,6R)-2-[C-[(2S)-butan-2-yl]-N-sulfonatooxy-carbonimidoyl]s ulfanyl-3,4,5-trihydroxy-6-(hydroxymethyl)oxane Preparation Products And Raw materials |
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