37527-70-1

Basic information

• Product Name: 2-(n-butylthio)benzyl alcohol
• Synonyms: 2-(n-butylthio)benzyl alcohol
• CAS NO: 37527-70-1
• Molecular Weight: 196.313
• Mol File: 37527-70-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(n-butylthio)benzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(n-butylthio)benzyl alcohol(37527-70-1)
• EPA Substance Registry System: 2-(n-butylthio)benzyl alcohol(37527-70-1)

Safety Data

• Hazardous Substances Data: 37527-70-1(Hazardous Substances Data)

Upstream product

• 17839-61-1 (S-butyl)-2-thiosalicylic acid 
• 109-65-9 1-bromo-butane 
• 4521-31-7 o-hydroxymethyl thiophenol 
• 6630-33-7 ortho-bromobenzaldehyde 
• 91827-97-3 n-butyl 2-formylphenyl sulfide 

Downstream Products

• 100789-97-7 n-butyl 2-(methoxymethyl)phenyl sulfide 
• 37527-75-6 (2-Butylsulfanyl-phenyl)-acetic acid 
• 37527-73-4 2-(2-(butylthio)phenyl)acetonitrile 
• 37527-77-8 (2-butylsulfanyl-phenyl)-acetic acid methyl ester 
• 37527-81-4 [2-(Butane-1-sulfinyl)-phenyl]-acetic acid methyl ester 
• 100790-03-2 n-butyl 2-(hydroxymethyl)phenyl sulfoxide 
• 37527-71-2 2-Butylthiobenzylchlorid 

Relevant articles and documents

Synthesis of 2,3-dihydrobenzo[b]thiophen-3-amine 1,1-dioxide derivatives via lda-mediated cyclization of o-(alkylsulfonyl)benzyl azides with denitrogenation

A new and efficient method for the synthesis of 2,3-dihydrobenzo[b]thiophen-3-amine 1,1-dioxide derivatives has been developed. Thus, treatment of o-(alkylsulfonyl)benzyl azides, which are readily obtainable from commercially available starting materials

5-LIPOXYGENASE INHIBITORS

This invention relates to 2-(substituted)-N-hydroxy-N-alkylcinnamamides of the formula: where R1 is C1 -C4 alkyl; n is 0 or 1; R2 is trifluoromethyl, C1 -C10 alkyl, phen(C1 -C4)alkylene or where m is 0, 1 or 2 and R3 is C1 -C4 alkyl; X is C1 -C6 alkyl, ph