Welcome to LookChem.com Sign In|Join Free
  • or
Indan-5-yl acetate, with the molecular formula C11H12O2, is a colorless liquid characterized by a sweet, floral odor. It is a versatile chemical compound that finds applications in various industries due to its distinctive scent and properties.

5440-82-4

Post Buying Request

5440-82-4 Suppliers

Recommended suppliers

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

5440-82-4 Usage

Uses

Used in Fragrance Industry:
Indan-5-yl acetate is used as a fragrance ingredient for its fruity and floral scent, enhancing the aroma of perfumes, soaps, and other personal care products.
Used in Flavor and Food Industry:
It serves as a flavoring agent in the production of food and beverages, adding a pleasant taste and aroma to a variety of consumer products.
Used in Fine Chemicals and Pharmaceuticals:
Indan-5-yl acetate is utilized in the manufacturing process of fine chemicals and pharmaceuticals, contributing to the development of various medicinal and chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 5440-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5440-82:
(6*5)+(5*4)+(4*4)+(3*0)+(2*8)+(1*2)=84
84 % 10 = 4
So 5440-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O2/c1-8(12)13-11-6-5-9-3-2-4-10(9)7-11/h5-7H,2-4H2,1H3

5440-82-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1H-inden-5-yl acetate

1.2 Other means of identification

Product number -
Other names acetic acid indan-5-ylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5440-82-4 SDS

5440-82-4Downstream Products

5440-82-4Relevant academic research and scientific papers

Copper-Catalyzed C-S Bond Formation via the Cleavage of C-O Bonds in the Presence of S8 as the Sulfur Source

Rostami, Abed,Rostami, Amin,Ghaderi, Arash,Gholinejad, Mohammad,Gheisarzadeh, Sajedeh

, p. 5025 - 5038 (2017/10/06)

Useful and applicable methods for one-pot and odorless synthesis of unsymmetrical and symmetrical diaryl sulfides via C-O bond activation are presented. First, a new efficient procedure for the synthesis of unsymmetrical sulfides using the cross-coupling reaction of phenolic esters such as acetates, tosylates, and triflates and with arylboronic acid or triphenyltin chloride as the coupling partners is reported. Depending on the reaction, S 8 /KF or S 8 /NaO t -Bu system is found to be an effective source of sulfur in the presence of copper salts and in poly(ethylene glycol) as a green solvent. Then, the synthesis of symmetrical diaryl sulfides from phenolic compounds by using S 8 as the sulfur source and NaO t -Bu in anhydrous DMF at 120 °C under N 2 is described. By these protocols, the synthesis of a variety of unsymmetrical and symmetrical sulfides become easier than the available protocols in which thiols and aryl halides are directly used for the preparation of the sulfides.

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 5440-82-4