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品質等級
化驗
≥95%
形狀
liquid
環保替代產品特色
Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
折射率
n/D 1.50625
密度
1.32 g/mL
環保替代類別
, Aligned
儲存溫度
2-8°C
SMILES 字串
[H][C@]1(C=CC2=O)CO[C@]2([H])O1
InChI
1S/C6H6O3/c7-5-2-1-4-3-8-6(5)9-4/h1-2,4,6H,3H2/t4-,6+/m0/s1
InChI 密鑰
HITOXZPZGPXYHY-UJURSFKZSA-N
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相关类别
一般說明
We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is biorenewable and thus aligns with ″Safer Solvents and Auxiliaries″ and ″Use of Renewable Feedstocks″. Click here for more information.
Levoglucosenone undergoes Michael-addition reaction with diethyl malonate, ethyl cyanoacetate, 2-nitropropane and 2-methylcyclohexanone in the presence of various catalysts to afford 4-substituted levoglucosenone derivatives having the D-erythro configuration.
Levoglucosenone undergoes Michael-addition reaction with diethyl malonate, ethyl cyanoacetate, 2-nitropropane and 2-methylcyclohexanone in the presence of various catalysts to afford 4-substituted levoglucosenone derivatives having the D-erythro configuration.
應用
Levoglucosenone may be used in the synthesis of the following:
- Various deoxy, keto and branched-chain sugars
- 4-thio and 4-substituted sugar derivatives
- Natural stereoisomer of serricornin
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
Levoglucosenone and Its New Applications: Valorization of Cellulose Residues.
European Journal of Organic Chemistry, 590-604 (2018)
Natural product reports, 37(3), 380-424 (2019-10-19)
Covering: up to mid-2019 This review highlights the utilization of biomass-derived building blocks in the total synthesis of natural products. An overview over several renewable feedstock classes, namely wood/lignin, cellulose, chitin and chitosan, fats and oils, as well as terpenes
Recent Applications of Levoglucosenone as Chiral Synthon.
Current Organic Synthesis, 9(4), 439-459 (2012)
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