72375-01-0

Basic information

• Product Name: 5-BENZYL-2-HYDROXY-BENZALDEHYDE
• Synonyms: 5-BENZYL-2-HYDROXY-BENZALDEHYDE
• CAS NO: 72375-01-0
• Molecular Formula: C₁₄H₁₂O₂
• Molecular Weight: 212.24
• Mol File: 72375-01-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-BENZYL-2-HYDROXY-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BENZYL-2-HYDROXY-BENZALDEHYDE(72375-01-0)
• EPA Substance Registry System: 5-BENZYL-2-HYDROXY-BENZALDEHYDE(72375-01-0)

Safety Data

• Hazardous Substances Data: 72375-01-0(Hazardous Substances Data)

Upstream product

• 101-53-1 p-benzylphenol 
• 67-66-3 chloroform 
• 100-44-7 benzyl chloride 
• 90-02-8 salicylaldehyde 
• 5896-17-3 2-(phenylmethoxy)benzaldehyde 
• 50-00-0 formaldehyd 
• 1761-61-1 5-bromosalicyclaldehyde 

Downstream Products

• 120233-03-6 bis-[4-(5-benzyl-2-hydroxy-benzylidenamino)-phenyl]-sulfoxide 
• 380542-05-2 5-benzyl-3-chlorosalicylaldehyde 
• 328565-15-7 5-benzyl-3-bromosalicylaldehyde 
• 101736-68-9 3-acetyl-6-benzyl-coumarin 
• 102077-78-1 6-benzyl-3-butyryl-coumarin 
• 108979-91-5 1-(5-benzyl-benzofuran-2-yl)-ethanone 
• 109614-98-4 6-benzyl-2-oxo-2H-chromene-3-carboxylic acid ethyl ester 
• 722493-91-6 5-benzyl-2-methoxy-benzaldehyde 
• 101277-94-5 6-benzylcoumarin 
• 1146296-45-8 C₁₄H₁₃NO₂ 
• 773021-13-9 5-benzylsalicylamine 
• 128236-89-5 C₁₄H₁₅NO*ClH 
• 328565-16-8 5-benzyl-2-hydroxy-3-nitrobenzaldehyde 

Relevant articles and documents

Structure-activity relationship study on col-003, a protein-protein interaction inhibitor between collagen and Hsp47

This study demonstrates the structure-activity relationship of Col-003, a potent collagen-heat-shock protein 47 (Hsp47) interaction inhibitor. Col-003 analogues were successfully synthesized by Pd(0)-catalyzed cross-coupling reactions of 5-bromosalicylald

Acidic rearrangement of (benzyloxy)chalcones: A short synthesis of chamanetin

Treatment of (benzyloxy)chalcones with trifluoroacetic acid in refluxing chloroform gave several new benzyl(hydroxy)flavanones in high yields and good regioselectivities. By using this procedure, we prepared the natural compound chamanetin in good yield from readily available reagents. Georg Thieme Verlag Stuttgart - New York.