70086-68-9 Usage
Uses
Used in Fragrance Industry:
Pentyl 2-chlorobenzoate is used as a fragrance ingredient for its unique scent profile, enhancing the aroma of various consumer products such as perfumes, colognes, and body care products.
Used in Flavoring Industry:
In the flavoring industry, pentyl 2-chlorobenzoate is employed as a flavor enhancer, imparting a distinct taste to food and beverage products, contributing to their overall flavor profile.
Used in Pharmaceutical Industry:
Pentyl 2-chlorobenzoate is utilized as a pharmaceutical intermediate, playing a crucial role in the synthesis of various drugs and medications, facilitating the development of new therapeutic agents.
Used in Organic Synthesis:
As a solvent in organic synthesis, pentyl 2-chlorobenzoate aids in various chemical reactions, enabling the production of a wide range of compounds for different applications.
Used in Chemical Intermediate Production:
Pentyl 2-chlorobenzoate serves as a chemical intermediate in the manufacturing process of other compounds, contributing to the synthesis of various industrial and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 70086-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70086-68:
(7*7)+(6*0)+(5*0)+(4*8)+(3*6)+(2*6)+(1*8)=119
119 % 10 = 9
So 70086-68-9 is a valid CAS Registry Number.
70086-68-9Relevant articles and documents
Solvent- and Metal-free Oxidative Esterification of Aromatic Aldehydes Using Urea-2,2-dihydroperoxypropane as a New Solid Oxidant
Khosravi, Kaveh,Khalaji, Kobra,Naserifar, Shirin
, p. 303 - 309 (2017/03/27)
Urea-2,2-dihydroperoxypropane as a noble and solid gem-dihydroperoxide derivative was used to transform various aromatic aldehydes to their corresponding benzoate derivatives in the presence of HBr under mild conditions at room temperature in high yields and short reaction times.
Iron(III) chloride-promoted direct conversion of aryl/alkyl cyanides to esters
Srinivasan,Rao, K. Srinivasa,Jayachitra,Ralte, Samuel L.
, p. 2883 - 2886 (2007/10/03)
Aryl/alkyl cyanides were quickly converted into the corresponding esters in the presence of iron(III) chloride in refluxing alcohols with very good yields. Copyright Taylor & Francis Group, LLC.
