40141-13-7

Basic information

• Product Name: Benzene, 1-butoxy-4-(chloromethyl)-
• CAS NO: 40141-13-7
• Molecular Formula: C11H15ClO
• Molecular Weight: 198.692
• Mol File: 40141-13-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-butoxy-4-(chloromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-butoxy-4-(chloromethyl)-(40141-13-7)
• EPA Substance Registry System: Benzene, 1-butoxy-4-(chloromethyl)-(40141-13-7)

Safety Data

• Hazardous Substances Data: 40141-13-7(Hazardous Substances Data)

Upstream product

• 6214-45-5 (4-butoxyphenyl)methanol 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 5736-88-9 p-butoxybenzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 1126-79-0 n-butyl phenyl ether 
• 4906-25-6 methyl 4-butyloxybenzoate 
• 99-76-3 methyl 4-hydroxylbenzoate 

Downstream Products

• 5736-88-9 p-butoxybenzaldehyde 
• 22699-14-5 1-butoxy-4-methoxymethyl-benzene 
• 21244-35-9 p-n-butoxybenzylamine 
• 155929-61-6 3,4,5-Tris-(4-butoxy-benzyloxy)-benzoic acid methyl ester 
• 198819-50-0 (4-Butoxy-benzyl)-phosphonic acid diethyl ester 
• 38746-93-9 2-(4-butoxyphenyl)acetonitrile 
• 60982-01-6 4-Butoxy-4'-butoxy-α-cyanostilben 
• 155929-55-8 3,4,5-tris(p-butoxybenzyloxy)benzoic acid 
• 146258-29-9 5-((E)-4-butoxystyryl)thiophene-2-carbaldehyde 

Relevant articles and documents

Structure-activity relationship (SAR) studies on the mutagenic properties of 2,7-diaminofluorene and 2,7-diaminocarbazole derivatives

We discovered that 2,7-diaminofluorene or 2,7-diaminocarbazole moiety can be employed as a core structure of highly effective NS5A inhibitors that are connected through amide bonds to proline-valine-carbamate motifs. Amide bonds can be easily cleaved via various metabolic pathways upon administration into the body, and metabolites containing 2,7-diaminofluorene and 2,7-diaminocarbazole core structures have been known to be strong mutagens. To avoid the mutagenesis issue of these core structures, we examined various functional groups at the C9 or N9 position of 2,7-diaminofluorene or 2,7-diaminocarbazole, respectively, through the Ames test in TA98 and TA100 mutants of Salmonella typhimurium LT-2. We discovered that, through proper alkyl substitution at the C9 or N9 position, 2,7-diaminofluorene and 2,7-diaminocarbazole moieties can be successfully employed in drug discovery without necessarily causing mutagenicity problems.

Amphiphilic dendritic dipeptides and their self-assembly into helical pores

An amphiphilic dendritic dipeptide, comprises a dipeptide(s) comprising one or more of a naturally occurring or synthetic amino acids and a dendron. These are suitable for use in various formulations, films, coatings, membranes and sensors, among other ap

Synthesis and characterization of end-functionalized oligo- (vinylthiophenes) with liquid crystal properties

A general scheme for the synthesis of end-functionalized conjugated (E)-vinylthiophene oligomers with liquid crystal and potential second-order non-linear optical properties is described. These push-pull thiophene-containing aromatic molecules show mesogenic properties over different temperature ranges depending on the chain length and the functional end-groups.