110683-66-4

Basic information

• Product Name: Benzenemethanol, 2-pentyl- (9CI)
• Synonyms: Benzenemethanol, 2-pentyl- (9CI)
• CAS NO: 110683-66-4
• Molecular Formula: C₁₂H₁₈O
• Molecular Weight: 178.27072
• Product Categories: PHENYL
• Mol File: 110683-66-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 266.6±8.0 °C(Predicted)
• Appearance: /
• Density: 0.960±0.06 g/cm3(Predicted)
• PKA: 14.39±0.10(Predicted)
• CAS DataBase Reference: Benzenemethanol, 2-pentyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-pentyl- (9CI)(110683-66-4)
• EPA Substance Registry System: Benzenemethanol, 2-pentyl- (9CI)(110683-66-4)

Safety Data

• Hazardous Substances Data: 110683-66-4(Hazardous Substances Data)

Upstream product

• 110683-65-3 ((E)-2-Pent-1-enyl)-benzoic acid methyl ester 
• 89-95-2 2-methyl-benzyl alcohol 
• 75-03-6 ethyl iodide 
• 109-65-9 1-bromo-butane 
• 4122-56-9 methyl o-formylbenzoate 
• 122654-40-4 4,4-Dimethyl-2-(2-pentyl-phenyl)-4,5-dihydro-oxazole 
• 693-25-4 n-pentylmagnesium bromide 
• 100368-67-0 2-Amyl-benzamid 
• 26311-42-2 2-n-pentylbenzoic acid 
• 57598-33-1 2-(2-methoxyphenyl)-4,4-dimethyl-2-oxazoline 
• 496-14-0 1,3-dihydroisobenzofuran 
• 180068-03-5 n-butyl phthalan 
• 26311-41-1 methyl o-amylbenzoate 

Downstream Products

• 26311-42-2 2-n-pentylbenzoic acid 
• 110683-35-7 o-amylcinnamic acid 
• 103175-75-3 4-Pentyl-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-benzamide 
• 103178-04-7 2-Pentyl-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-benzamide 
• 110698-31-2 (E)-3-(2-Pentyl-phenyl)-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-acrylamide 
• 151888-64-1 2-Diphenylacetyl-5-pentyl-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester 
• 1026260-46-7 2-Formylamino-2-(2-pentyl-benzyl)-malonic acid diethyl ester 
• 59059-43-7 2-n-pentylbenzaldehyde 
• 1026802-35-6 Methanesulfonic acid 2-pentyl-benzyl ester 

Relevant articles and documents

COMPOUNDS REDUCING MALODOUR PERCEPTION AND THE USE THEREOF

The present invention relates to new malodour-counteracting agents of formula (I) or stereoisomers thereof, particularly useful in blocking the olfactory perception of androstenone, Formula (I), wherein R1, R2, R3,R4, R5, R6, R7 and X have the same meaning as that defined in the claims. The present invention also relates to consumer products comprising said agents. The present invention also relates to the use of said agents to suppress or attenuate undesirable odour, as well as to methods to suppress or attenuate undesirable odour employing said compounds.

Electron-transfer-induced reductive cleavage of phthalans: Reactivity and synthetic applications

The behavior of phthalan (1a) was investigated under conditions of electron transfer from alkali metals in aprotic solvents. Reaction with lithium in the presence of a catalytic amount of naphthalene in THF led to the reductive cleavage of an arylmethyl carbon-oxygen bond, with formation of a stable dilithium compound. Trapping of this intermediate with several electrophiles (alkyl halides, carbonyl derivatives, CO2) was successful. The extension of this procedure to several substituted phthalans (1b-i) was investigated, and the regiochemistry as well as the synthetic usefulness of these reactions are discussed.

Leukotriene-B4 derivatives, process for their production and their use as pharmaceutical agents

STR1 Compounds of formula (I) in which the residues have the following meanings: a is (II) or (III); R1 is CH2 OH, CH3, CF3, COOR5 with R5 or, A is a trans, trans--CH=CH--CH=CH--or tetramet