CAS: 18918-31-5; (2S,3R,4R,5R,6S)-2-Methyl-6-(4-Nitrophenoxy)Tetrahydro-2H-Pyran-3,4,5-Triol
该化合物是一个化学化合物,用作甘蓝的基质,特别是甘蔗糖的衍生物.它有一个p-硝基苯组,这是生物化学实验中常用的染色素,使该化合物在各种应用中,特别是在酶学研究中有用.结构包括一个通过甘油粘合剂与p-硝基苯组相连的红蛋白质单位.该化合物通常用作甘油酶的基质,使研究人员能够研究酶动力学和机制.其特点是其在极地溶剂中的溶性,其再活动性可能受到周围环境中功能组的存在的影响.此外,p-硝基苯基苯基分子的混合物可以通过特定的酶,释放p-nicetencils进行水解.该化合物可以定量测量,提供酶化学活动的色度指示.
- 英文名称(2S,3R,4R,5R,6S)-2-Methyl-6-(4-Nitrophenoxy)Tetrahydro-2H-Pyran-3,4,5-Triol
- 中文名称4-硝基苯基-Α-L-吡喃鼠李糖苷
- IUPAC名称(2S,3R,4R,5R,6S)-2-methyl-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol
- 其它别名4-Nitrophenylrhamnoside ; 4-Nitrophenyl-Alpha-L-Rhamnoside ; (2S,3R,4R,5R,6S)-2-Methyl-6-(4-Nitrophenoxy)Oxane-3,4,5-Triol ; 3-Nitrophenyl A-L-Rhamnopyranoside ; 4-Nitrophenyl A-L-Rhamnopyranoside ; 4-Nitrophenyl Alpha-L-Rhamnopyranoside
- CAS编号18918-31-5
- MFCD编号:MFCD00069788
- 分子式:C12H15NO7分子量:285.25
- 产品CID: 958706
- 产品分类有机原料→生命科学→生化试剂→酶底物
相似化合物
35599-02-1 3767-28-0 2492-87-7物理性质
MSDS等安全信息
上下游产品
4-nitrophenyl-2,3,4,6-tetra-O-acetyl-α-L-rhamnopyranoside 4-nitro-phenol 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl chloride1-(4-aminophenoxy)-α-L-rhamnopyranoside p-nitrophenyl 2,3-O-isopropylidene-α-L-rhamnopyranoside p-nitrophenyl 4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-glucopyranosyl)-2,3-O-isopropylidene-α-L-rhamnopyranoside p-nitrophenyl 2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside合成工艺路线路线简述
📜P-Nitrophenyl 2,3,4-Tri-O-Acetyl-α-L-Rhamnopyranoside置于甲醇,Sodium Methylate体系中,化学反应生成对硝基苯基-Alpha-L-吡喃鼠李糖苷
参考文献:Westphal; Feier,Chemische Berichte,1956,Vol. 89,P. 582,587
标题:Westphal; Feier,Chemische Berichte,1956,Vol. 89,P. 582,587
海关参考信息
- 2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-100486984-C
优先权日:2007-06-06
标题:Synthesis of p-nitrophenyl α-L-rhamnoside
专利号:CN-101058593-A
优先权日:2007-06-06
标题 :Synthesis of p-nitrophenyl α-L-rhamnoside
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Synthesis Of Allyl And Benzyl 4-O-(3,6-Di-O-Methyl-β-D-Glucopyranosyl)-2,3-Di-O-Methyl-α-L-Rhamnopyranoside作者:Jose R. Mariño-Albernas,Vicente Verez-Bencomo,Leandro Gonzalez,Carlos S. Perez |发布日期:1987.8
摘要:Abstract Condensation Of 2,4-Di- O -Acetyl-3,6-Di- O -Methyl-α- D -Glucopyranosyl Bromide With Either Allyl Or Benzyl 2,4-Di- O -Methyl-α- L -Rhamnopyranoside In The Presence Of Mercuric Cyanide, Followed By O -Deacetylation, Gave The Title Oligosaccharides In Excellent Yields.
合成参考文献
参考文献:10.1007/s12010-019-03063-5
摘要:Li BC, Zhang T, Li YQ, Ding GB. Target Discovery of Novel α-L-Rhamnosidases from Human Fecal Metagenome and Application for Biotransformation of Natural Flavonoid Glycosides. Appl Biochem Biotechnol. 2019 Dec;189(4):1245–61. doi: 10.1007/s12010-019-03063-5.
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