15181-07-4

Basic information

• Product Name: 1-heptyl-4-methylbenzene
• Synonyms: 1-Heptyl-4-methylbenzene; Benzene, 1-heptyl-4-methyl; benzene, 1-heptyl-4-methyl-
• CAS NO: 15181-07-4
• Molecular Formula: C₁₄H₂₂
• Molecular Weight: 190.3245
• Mol File: 15181-07-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 264.4°C at 760 mmHg
• Flash Point: 113.6°C
• Density: 0.86g/cm³
• Vapor Pressure: 0.0159mmHg at 25°C
• Refractive Index: 1.488
• CAS DataBase Reference: 1-heptyl-4-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-heptyl-4-methylbenzene(15181-07-4)
• EPA Substance Registry System: 1-heptyl-4-methylbenzene(15181-07-4)

Safety Data

• Hazardous Substances Data: 15181-07-4(Hazardous Substances Data)

Upstream product

• 629-04-9 1-Bromoheptane 
• 5720-05-8 4-methylphenylboronic acid 
• 141-52-6 sodium ethanolate 
• 2528-61-2 Heptanoic acid chloride 
• 108-88-3 toluene 

Downstream Products

• 4517-99-1 Wy 41770 

Relevant articles and documents

PROCESS FOR PRODUCING PHOSPHONIUM BORATE COMPOUND, NOVEL PHOSPHONIUM BORATE COMPOUND, AND METHOD OF USING THE SAME

The invention relates to a phosphonium borate compound represented by Formula (I) (hereinafter, the compound (I)). The invention has objects of providing (A) a novel process whereby the compound is produced safely on an industrial scale, by simple reaction operations and in a high yield; (B) a novel compound that is easily handled; and (C) novel use as catalyst. ????????Formula (I) : (R1)(R2)(R3)PH·BAr4?????(I) wherein R1, R2, R3 and Ar are as defined in the specification. The process (A) includes reacting a phosphine with a) HCl or b) H2SO4 to produce a) a hydrochloride or b) a sulfate; and reacting the salt with a tetraarylborate compound. The compound (B) has for example a secondary or tertiary alkyl group as R1 and is easily handled in air without special attention. The use (C) is characterized in that the compound (I) is used instead of an unstable phosphine compound of a transition metal complex catalyst for catalyzing C-C bond, C-N bond and C-O bond forming reactions and the compound produces an effect that is equal to that achieved by the transition metal complex catalyst.