Welcome to LookChem.com Sign In|Join Free
  • or
α-(9-anthryl)benzyl methyl ether is a synthetic organic compound characterized by its molecular formula C19H16O. It is a derivative of benzyl methyl ether, with a 9-anthryl group attached to the alpha carbon of the benzyl moiety. α-(9-anthryl)benzyl methyl ether is known for its unique photophysical properties, particularly its fluorescence, which makes it a potential candidate for applications in the field of fluorescence sensing and imaging. The 9-anthryl group provides a significant chromophore, enhancing the compound's ability to absorb and emit light, which is valuable in various analytical and diagnostic techniques. Its chemical structure and properties also make it a subject of interest in organic chemistry research, particularly in the study of aromatic compounds and their interactions.

2026-30-4

Post Buying Request

2026-30-4 Suppliers

Recommended suppliers

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

2026-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2026-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2026-30:
(6*2)+(5*0)+(4*2)+(3*6)+(2*3)+(1*0)=44
44 % 10 = 4
So 2026-30-4 is a valid CAS Registry Number.

2026-30-4Downstream Products

2026-30-4Relevant academic research and scientific papers

Reaction of (9-anthryl)arylmethyl Chlorides with Grignard and Lithium Reagents

Takagi, Masato,Nojima, Masatomo,Kusabayashi, Shigekazu

, p. 1636 - 1643 (2007/10/02)

We have investigated the reaction of (9-anthryl)arylmethyl chlorides 1a-d (para substituent = MeO, Me, H, and Cl) with Grignard and lithium reagents.The variables are the structures of the alkyl group of Grignard and lithium reagents (alkyl group = tert-b

Reactions of (9-Anthryl)arylmethyl Chloride and Its Homologues with Nucleophiles under Solvolytic Conditions. Notable Effects of Reaction Conditions and Substituents on the Reaction Sites

Ogata, Fujimaro,Takagi, Masato,Nojima, Masatomo,Kusabayashi, Shigekazu

, p. 1145 - 1153 (2007/10/02)

The reactions of (9-anthryl)arylmethyl chlorides 2a-e (the substituents are p-MeO, p-Me, H, p-Cl, and m-Cl), the corresponding bromides 3b-d (the substituents are p-Me, H, and p-Cl), and the antimonate salts 4b-e (the substituents are p-Me, H, p-Cl, and m

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 2026-30-4