1346458-85-2

Basic information

• Product Name: C₂₂H₂₅ClO₁₀
• Synonyms: C₂₂H₂₅ClO₁₀
• CAS NO: 1346458-85-2
• Molecular Weight: 484.888
• Mol File: 1346458-85-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₂H₂₅ClO₁₀(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₂H₂₅ClO₁₀(1346458-85-2)
• EPA Substance Registry System: C₂₂H₂₅ClO₁₀(1346458-85-2)

Safety Data

• Hazardous Substances Data: 1346458-85-2(Hazardous Substances Data)

Upstream product

• 261958-55-8 2,4-dihydroxy-6-[(phenylmethoxy)methyl]-benzaldehyde 
• 82265-37-0 1,3-bis(methoxymethoxy)-5-methylbenzene 
• 1320259-78-6 3-chloro-2-hydroxy-4-methoxy-6-[(phenylmethoxy)methyl]-benzaldehyde 
• 1320259-48-0 2-hydroxy-4-methoxy-6-[(phenylmethoxy)methyl]-benzaldehyde 
• 1320259-75-3 C₂₂H₂₅ClO₉ 
• 1320259-70-8 [2,6-bis(methoxymethoxy)-4-methylphenyl][3-chloro-6-hydroxymethyl-4-methoxy-2-(methoxymethoxy)phenyl]-methanone 
• 1320259-68-4 [2,6-bis(methoxymethoxy)-4-methylphenyl][3-chloro-4-methoxy-2-(methoxymethoxy)-6-[(phenylmethoxy)methyl]phenyl]-methanone 
• 1320259-67-3 2,6-bis(methoxymethoxy)-α-[3-chloro-4-methoxy-2-methoxymethoxy-6-[(phenylmethoxy)-methyl]]-4-methyl-benzenemethanol 
• 1320259-65-1 3-chloro-4-methoxy-2-methoxymethoxy6-[(phenylmethoxy)methyl]-benzaldehyde 

Downstream Products

• 1320259-68-4 [2,6-bis(methoxymethoxy)-4-methylphenyl][3-chloro-4-methoxy-2-(methoxymethoxy)-6-[(phenylmethoxy)methyl]phenyl]-methanone 
• 1320259-70-8 [2,6-bis(methoxymethoxy)-4-methylphenyl][3-chloro-6-hydroxymethyl-4-methoxy-2-(methoxymethoxy)phenyl]-methanone 
• 1346458-46-5 C₂₂H₂₇ClO₉ 
• 1320259-71-9 C₂₂H₂₇ClO₈ 
• 165905-02-2 methyl 2-(2-carboxy-3-hydroxy-5-methylphenoxy)-4-chloro-3-hydroxy-5-methoxybenzoate 
• 1320259-72-0 methyl 2-[2,6-bis(methoxymethoxy)-4-methylbenzoyl]-4-chloro-5-methoxy-3-methoxymethoxy-benzoat 

Relevant articles and documents

Syntheses of chloroisosulochrin and isosulochrin and biomimetic elaboration to maldoxin, maldoxone, dihydromaldoxin, and dechlorodihydromaldoxin

An efficient synthesis of chloroisosulochrin was accomplished using a novel ortho-selective chlorination of a phenol with sulfuryl chloride and 2,2,6,6-tetramethylpiperidine as the key step. Further elaboration by a biomimetic route converted chloroisosul