Welcome to LookChem.com Sign In|Join Free
  • or
2-Naphthalenecarboxylic acid, heptyl ester, also known as 2-naphthoic acid heptyl ester or heptyl 2-naphthoate, is an organic compound with the chemical formula C17H20O2. It is a colorless to pale yellow liquid with a molecular weight of 256.34 g/mol. This ester is formed by the reaction of 2-naphthoic acid with heptyl alcohol, resulting in an esterification process. The compound is characterized by its aromatic structure, with a naphthalene ring and a heptyl chain attached to the carboxylic acid group. It is used in various applications, such as a fragrance ingredient in perfumes and as a chemical intermediate in the synthesis of other organic compounds. Due to its chemical structure, it exhibits properties like low solubility in water and high solubility in organic solvents.

2876-79-1

Post Buying Request

2876-79-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2876-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2876-79-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2876-79:
(6*2)+(5*8)+(4*7)+(3*6)+(2*7)+(1*9)=121
121 % 10 = 1
So 2876-79-1 is a valid CAS Registry Number.

2876-79-1Downstream Products

2876-79-1Relevant academic research and scientific papers

Pd/C-Catalyzed Carbonylative Esterification of Aryl Halides with Alcohols by Using Oxiranes as CO Sources

Min, Byul-Hana,Kim, Dong-Su,Park, Hyo-Soon,Jun, Chul-Ho

supporting information, p. 6234 - 6238 (2016/05/02)

A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. In this process, oxiranes serve as sources of carbon monoxide by their conversion to aldehydes through a palladium-promoted Meinwald rearrangement pathway. Intramolecular versions of this process serve as methods for the synthesis of lactones and phthalimides. CO gas free! A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. In this process, oxiranes serve as sources of carbon monoxide by their conversion to aldehydes through a palladium-promoted Meinwald rearrangement pathway (see scheme).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2876-79-1