137575-62-3 Usage
Chemical Class
Diols and Phenols
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)belongs to the class of diols and phenols, which are organic compounds containing two or more hydroxyl (-OH) groups attached to a benzene ring.
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)- is widely used as a solvent due to its ability to dissolve various substances. It is also utilized in the production of chemicals, plastics, textiles, and personal care products, thanks to its unique properties.
Explanation
The presence of the 1-(4-chlorophenyl) group in the butanediol molecule contributes to its specific properties, making it suitable for various applications in different industries.
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)can be used as a starting material or precursor in the synthesis of pharmaceuticals and other organic compounds, due to its unique chemical structure.
Explanation
This chemical compound can have toxic effects if not used properly, so it is essential to handle it with care and follow safety guidelines to minimize potential health risks.
Explanation
The molecular formula of 1,4-Butanediol, 1-(4-chlorophenyl)is C10H13ClO2, indicating the presence of carbon (C), hydrogen (H), chlorine (Cl), and oxygen (O) atoms in the molecule.
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)- is typically found in a liquid state at room temperature, which makes it suitable for use as a solvent and in various chemical reactions.
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)is soluble in organic solvents such as ethanol, methanol, and acetone, which contributes to its utility as a solvent in various applications.
Explanation
1,4-Butanediol, 1-(4-chlorophenyl)- is generally stable under normal conditions, such as room temperature and pressure, making it suitable for use in various industrial processes.
Explanation
To maintain the stability and safety of 1,4-Butanediol, 1-(4-chlorophenyl)-, it should be stored in a cool, dry place, away from direct sunlight, heat, and moisture.
Common Uses
Solvent, Chemical Production, Plastics, Textiles, and Personal Care Products
1-(4-chlorophenyl) Group
Adds Specific Properties
Precursor in Synthesis
Pharmaceuticals and Organic Compounds
Toxicity
Handle with Caution
Molecular Structure
C10H13ClO2
Physical State
Liquid
Solubility
Soluble in Organic Solvents
Stability
Stable under Normal Conditions
Storage
Keep in a Cool, Dry Place
Check Digit Verification of cas no
The CAS Registry Mumber 137575-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,5,7 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137575-62:
(8*1)+(7*3)+(6*7)+(5*5)+(4*7)+(3*5)+(2*6)+(1*2)=153
153 % 10 = 3
So 137575-62-3 is a valid CAS Registry Number.
137575-62-3Relevant academic research and scientific papers
Aryl Boronic Acid Catalysed Dehydrative Substitution of Benzylic Alcohols for C?O Bond Formation
Estopi?á-Durán, Susana,Donnelly, Liam J.,Mclean, Euan B.,Hockin, Bryony M.,Slawin, Alexandra M. Z.,Taylor, James E.
, p. 3950 - 3956 (2019/02/16)
A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitution of benzylic alcohols with a second alcohol to form new C?O bonds. This method has been applied to the intermolecular substitution of benzylic alcohols to form symmetrical ethers, intramolecular cyclisations of diols to form aryl-substituted tetrahydrofuran and tetrahydropyran derivatives, and intermolecular crossed-etherification reactions between two different alcohols. Mechanistic control experiments have identified a potential catalytic intermediate formed between the aryl boronic acid and oxalic acid.
Application of a one-pot lipase resolution strategy for the synthesis of chiral γ- and δ-lactones
Kamal, Ahmed,Sandbhor, Mahendra,Shaik, Ahmad Ali
, p. 1575 - 1580 (2007/10/03)
A successful one-pot reduction of γ-ketoesters, δ-ketoesters and lactones to the corresponding 1,4- and 1,5-diols followed by a lipase catalyzed kinetic resolution coupled with hydrolysis to afford optically active diols is described. The synthetic utility of this one-pot method was illustrated by the oxidation of these chiral diols to respective chiral γ-butyrolactone and δ-lactones. Lipase from Pseudomonas cepacia, immobilized on ceramic afforded the product with high enantiomeric excess in good yields under mild reaction conditions. This approach has been used to develop a convenient enantioselective route for several γ- and δ-lactones using achiral and corresponding racemic starting material.
