256464-90-1

Basic information

• Product Name: (2R,3R)-3,6-Bis-benzyloxy-2-methyl-hexanal
• Synonyms: (2R,3R)-3,6-Bis-benzyloxy-2-methyl-hexanal
• CAS NO: 256464-90-1
• Molecular Weight: 326.436
• Mol File: 256464-90-1.mol

Chemical Properties

• CAS DataBase Reference: (2R,3R)-3,6-Bis-benzyloxy-2-methyl-hexanal(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-3,6-Bis-benzyloxy-2-methyl-hexanal(256464-90-1)
• EPA Substance Registry System: (2R,3R)-3,6-Bis-benzyloxy-2-methyl-hexanal(256464-90-1)

Safety Data

• Hazardous Substances Data: 256464-90-1(Hazardous Substances Data)

Upstream product

• 256464-89-8 (3S,4R)-4,7-Bis-benzyloxy-3-methyl-heptane-1,2-diol 
• 256464-87-6 (3S,4R)-7-(benzyloxy)-3-methylhept-1-en-4-ol 
• 100-39-0 benzyl bromide 
• 4541-14-4 4-benzyloxy-butan-1-ol 
• 5470-84-8 4-benzyloxybutanal 
• 256464-88-7 C₂₂H₂₈O₂ 

Downstream Products

• 256464-91-2 C₂₅H₃₄O₃ 
• 256464-94-5 C₃₉H₄₈O₆S 
• 256464-95-6 C₃₃H₄₁NO₃ 
• 256464-96-7 C₃₃H₄₂O₄ 
• 256464-97-8 C₃₃H₄₄O₄ 
• 256464-92-3 C₃₂H₄₀O₃ 
• 256464-93-4 C₃₂H₄₂O₄ 
• 115566-02-4 bistramide A 
• 887612-26-2 2-{3-[(2R,3S,6S,8S)-8-[(S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutyl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]propyl}isoindoline-1,3-dione 
• 887612-10-4 3-((2R,3S,6S,8S)-8-[(S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutyl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl)propan-1-ol 
• 887612-09-1 C₂₂H₂₆O₂ 
• 887612-21-7 C₂₂H₂₆Br₂O₂ 

Relevant articles and documents

Enantioselective total synthesis of bistramide A

The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 18 steps. The synthetic strategy involves the use of a distereoselective glycolate alkylation, an aldol addition of a chlorotitanium enolate of N-acylthiazolidinthione, and a Sharpless asymmetric epoxidation to synthesize the three key fragments. Copyright

Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: Proof of concept

Oasomycin B: R = α-D-mannosyl Using the C.5-C.10 portion of the oasomycin class of natural products, the reliability and usefulness of an NMR database for the stereochemical assignment of acyclic compounds has been demonstrated. The predicted relative stereochemistry based on the NMR database has unambiguously been established via synthesis.