Welcome to LookChem.com Sign In|Join Free

CAS

  • or

24083-11-2

Post Buying Request

24083-11-2 Suppliers

Recommended suppliersmore

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

24083-11-2 Usage

General Description

2-(octyloxy)benzaldehyde is a chemical compound with the molecular formula C15H20O2. It is a type of benzaldehyde with an octyloxy group attached to the benzene ring. This chemical is commonly used in the production of fragrances, flavorings, and as a synthetic building block in organic chemistry. It is a pale yellow liquid with a sweet, floral odor, and is often used in perfumes and cosmetic products. Additionally, 2-(octyloxy)benzaldehyde has been studied for its potential antimicrobial and antioxidant properties, making it a versatile and valuable chemical in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24083-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,8 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24083-11:
(7*2)+(6*4)+(5*0)+(4*8)+(3*3)+(2*1)+(1*1)=82
82 % 10 = 2
So 24083-11-2 is a valid CAS Registry Number.

24083-11-2Relevant articles and documents

Highly improved performance of ZnII tetraarylporphyrinates in DSSCs by the presence of octyloxy chains in the aryl rings

Orbelli Biroli,Tessore,Vece,Di Carlo,Mussini,Trifiletti,De Marco,Giannuzzi,Manca,Pizzotti

, p. 2954 - 2959 (2015)

Three new β-substituted ZnII-tetraarylporphyrinate dyes (1-3), bearing octyloxy chains at the o,o-, o,p- or o-positions of the four phenyl groups respectively, were synthesized, characterized and investigated as sensitizers for DSSCs. In particular, the alkoxy group position strongly influences their electronic absorption and electrochemical features. Improvements in power conversion efficiency ranging from 40% to 80% were obtained with respect to a reference dye (4) characterized by the presence of sterically bulky t-butyl groups at the m-positions.

Alkoxy substituted D-π-A dimethyl-4-pyrone derivatives: Aggregation induced emission enhancement, mechanochromic and solvatochromic properties

Cao, YuQi,Xi, Ye,Teng, XinYu,Li, Yang,Yan, Xilong,Chen, Ligong

, p. 75 - 83 (2016/10/25)

Three series of D-π-A 2,6-dimethyl-4-pyrone-cored derivatives were designed and synthesized. Evaluation by spectroscopic methods indicated that all the compounds exhibited aggregation-induced emission enhancement (AIEE) effect and solvatochromism. The experimental results revealed that the restriction of intramolecular rotation is the key element for showcasing the AIEE phenomenon. Moreover, all of the compounds presented red-shifted mechanochromic behavior, the extent of the red-shift was mainly dependent on the position and length of alkoxyl group. The PXRD and DSC profiles demonstrated a transformation from crystalline to amorphous state upon grinding. The D-A strategy introduced in this work could facilitate the development and application of ingenious mechanochromic materials.

Antiviral potentials. XII. Glycidic esters

Ulian,Vio

, p. 518 - 521 (2007/10/08)

-

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

What can I do for you?
Get Best Price

Get Best Price for 24083-11-2