51241-39-5 Usage
Chemical structure
1-chloro-2-(pentyloxy)benzene is an organic chemical compound with a benzene ring, a chlorine atom attached at the 1st position, and a pentyloxy group attached at the 2nd position.
Functional groups
The compound contains a chloro group (-Cl) and a pentyloxy group (-OCH2(CH2)3CH3).
Applications
It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.
Toxicity
1-chloro-2-(pentyloxy)benzene is known to have moderate toxicity.
Safety precautions
It is important to follow proper safety protocols when working with 1-chloro-2-(pentyloxy)benzene to minimize the risk of exposure and adverse health effects.
Physical state
As an organic compound, it is likely to be in a liquid or solid state at room temperature.
Solubility
It may be soluble in organic solvents such as ethanol, methanol, or acetone, due to its nonpolar nature.
Boiling point
The boiling point of 1-chloro-2-(pentyloxy)benzene is not provided, but it can be estimated based on the molecular weight and structure.
Melting point
The melting point of 1-chloro-2-(pentyloxy)benzene is not provided, but it can be estimated based on the molecular weight and structure.
Molecular weight
The molecular weight can be calculated from the molecular formula (C11H15ClO).
Reactivity
1-chloro-2-(pentyloxy)benzene may undergo various chemical reactions, such as substitution, elimination, or addition reactions, depending on the reaction conditions and reagents used.
Stability
The stability of 1-chloro-2-(pentyloxy)benzene may depend on factors such as temperature, exposure to light, and the presence of other reactive substances.
Storage
It should be stored in a cool, dry, and well-ventilated area, away from incompatible substances, and in a sealed container to prevent contamination and degradation.
Disposal
Proper disposal methods should be followed, such as neutralization, incineration, or recycling, to minimize environmental impact and ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 51241-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,4 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51241-39:
(7*5)+(6*1)+(5*2)+(4*4)+(3*1)+(2*3)+(1*9)=85
85 % 10 = 5
So 51241-39-5 is a valid CAS Registry Number.
51241-39-5Relevant academic research and scientific papers
Kodomari, Mitsuo,Takahashi, Shin,Yoshitomi, Suehiko
, p. 1901 - 1902 (1987)
Alkoxybenzenes were highly regioselectively chlorinated by use of copper(II) chloride supported on neutral alumina in chlorobenzene to give p-alkoxychlorobenzenes in high yield.The p/o ratios were more than 30.
Monohalogenation of alkyl phenyl ethers in micellar and vesicular media
Jaeger, David A.,Clennan, Malgorzata Wegrzyn,Jamrozik, Janusz
, p. 1171 - 1176 (2007/10/02)
The rates and regioselectivities of monohalogenation of C6H5OR (1: a, R = C5H11;b, R = C9H19; c, R = C12H25) by chlorine water and bromine water to give 4-XC6/su
SELECTIVITY OF AROMATIC CHLORINATION REACTIONS WITHIN A REVERSED-PHASE LIQUID CHROMATOGRAPHY COLUMN
Jaeger, David A.,Clennan, Malgorzata Wegrzyn,Leyden, Donald E.,Murthy, R. S. Shreedhara
, p. 4805 - 4808 (2007/10/02)
Substrate selectivity was obtained in the chlorination of a series of n-alkyl phenyl ethers by chlorine water on a reversed-phase high performance liquid chromatography column at 25 deg C.
Monochlorination of n-Alkyl Phenyl Ethers in Micellar Sodium Dodecyl Sulfate
Jaeger, David A.,Wyatt, Jacqueline R.,Robertson, Raymond E.
, p. 1467 - 1470 (2007/10/02)
The effect of chain length on the regioselectivity and rate of monochlorination of C6H5OR (1: a = n-C5H11; b, R = n-C9H19; c, R = n-C12H25) with Cl2 in micellar sodium dodecyl sulfate was determined.On going from 1a to 1b to 1c, only modest changes were observed in the para/ortho product ratio and in relative rate.These results were interpreted to indicate that the hydrophilic character of C6H5O dominates the lipophilic character of R in the micellar reactivity of the ethers.
POLY(ETHYLENE GLYCOL)S AS PHASE TRANSFER CATALYSTS IN THE ALKOXYLATION OF HALOBENZENES OF ALKYL ARYL ETHERS
Neumann, R.,Sasson, Y.
, p. 3437 - 3440 (2007/10/02)
Mono and di-halobenzenes and alkoxide ions gave monoalkoxybenzenes, but no phenols, when catalyzed by high molecular weight poly(ethylene glycol)s as phase transfer catalysts.Bromobenzenes were more reactive than chlorobenzenes but gave more side products, and for alcohols the reactivity was primary>secondary>tertiary.
