42400-32-8

Basic information

• Product Name: 2-Deoxy-D-arabino-hexonic acid 1,4-lactone
• Synonyms: 2-Deoxy-D-arabino-hexonic acid 1,4-lactone;2-Deoxy-D-arabino-hexonic acid γ-lactone
• CAS NO: 42400-32-8
• Molecular Formula: C6H10O5
• Molecular Weight: 162.14
• Mol File: 42400-32-8.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Deoxy-D-arabino-hexonic acid 1,4-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Deoxy-D-arabino-hexonic acid 1,4-lactone(42400-32-8)
• EPA Substance Registry System: 2-Deoxy-D-arabino-hexonic acid 1,4-lactone(42400-32-8)

Safety Data

• Hazardous Substances Data: 42400-32-8(Hazardous Substances Data)

Upstream product

• 5729-75-9 3-deoxy-D-gluconic acid 
• 61-58-5 2-deoxy-D-arabino-hexopyranose 
• 905708-49-8 2-O-benzoyl-D-glucono-1,4-lactone 
• 530-26-7 D-Mannose 
• 2280-44-6 D-Glucose 
• 69863-80-5 3,5,6-tri-O-acetyl-D-glucono-1,4-lactone 
• 2873-29-2 D-glucal triacetate 
• 1169836-00-3 C₁₃H₂₄O₆ 
• 71672-01-0 6-bromo-2,6-dideoxy-D-arabino-hexono-1,4-lactone 
• 69617-72-7 (3S,4S,5R,1'S)-3-bromo-5-(2'-bromo-1'-hydroxy)ethyl-4,5-dihydro-4-hydroxy-2-(3H)-furanone 
• 1198-69-2 D-glucono-1,4-lactone 
• 100227-29-0 5,6-di-O-isopropylidene-D-glucono-1,4-lactone 
• 905708-56-7 5,6-di-O-isopropylidene-2-O-[3-(trifluoromethyl)benzoyl]-D-glucono-1,4-lactone 
• 106182-88-1 1,6-di-O-(p-tolylsulfonyl)-D-fructose 

Downstream Products

• 61244-22-2 N-phenyl-2-deoxy-D-gluconohydrazide 

Relevant articles and documents

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A highly selective Bi(OTf)3 mediated fragmentation-contraction of δ-ortholactones. A facile route to functionalized γ-lactones

A very selective method for the formation of γ-lactones from pyranyl ortholactones has been developed which occurs via a fragmentation-acetate migration-ring contraction process. The reaction is very functional group tolerant, providing functionalized γ-l

Photoinduced electron-transfer α-deoxygenation of aldonolactones. Efficient synthesis of 2-deoxy-d-arabino-hexono-1,4-lactone

A photoinduced electron-transfer (PET) reaction was used for the deoxygenation at C-2 of aldonolactones derivatized as 2-O-[3-(trifluoromethyl)benzoyl] or benzoyl esters. By irradiation of different d-galactono- and d-glucono-1,4-derivatives, with a 450 W