25458-49-5 Usage
Description
1-(Methoxymethoxy)-4-methylbenzene, also known as 4-methoxy-1-(methoxymethoxy)benzene, is a chemical compound with the molecular formula C9H12O2. It is a colorless to light yellow liquid characterized by a sweet, floral odor. This versatile chemical is valued for its applications in various industries due to its distinct properties.
Uses
Used in Fragrance Industry:
1-(Methoxymethoxy)-4-methylbenzene is used as a fragrance ingredient for its sweet, floral scent, contributing to the creation of perfumes, cosmetics, and personal care products. Its unique aroma profile makes it a valuable addition to the fragrance industry.
Used in Food Industry:
In the food industry, 1-(Methoxymethoxy)-4-methylbenzene is utilized as a flavoring agent to enhance the taste and aroma of various food products, providing a pleasant sensory experience for consumers.
Used in Chemical Synthesis:
1-(Methoxymethoxy)-4-methylbenzene also serves as an intermediate in the synthesis of other chemical compounds, playing a crucial role in the production of various chemical products.
However, it is essential to handle 1-(Methoxymethoxy)-4-methylbenzene with care due to its potential hazards. It can be harmful if ingested, inhaled, or absorbed through the skin, and it may cause irritation to the eyes and skin upon contact. Proper safety measures should be taken to minimize risks during its use in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25458-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25458-49:
(7*2)+(6*5)+(5*4)+(4*5)+(3*8)+(2*4)+(1*9)=125
125 % 10 = 5
So 25458-49-5 is a valid CAS Registry Number.
25458-49-5Relevant articles and documents
Enantiodivergent Atroposelective Synthesis of Chiral Biaryls by Asymmetric Transfer Hydrogenation: Chiral Phosphoric Acid Catalyzed Dynamic Kinetic Resolution
Mori, Keiji,Itakura, Tsubasa,Akiyama, Takahiko
supporting information, p. 11642 - 11646 (2016/10/24)
Reported herein is an enantiodivergent synthesis of chiral biaryls by a chiral phosphoric acid catalyzed asymmetric transfer hydrogenation reaction. Upon treatment of biaryl lactols with aromatic amines and a Hantzsch ester in the presence of chiral phosp
Rational design of latent fluorophores from water-soluble hydroxyphenyltriazine dyes suitable for lipase sensing
Jacquemet, Alicia,Rihn, Sandra,Ulrich, Gilles,Renard, Pierre-Yves,Romieu, Anthony,Ziessel, Raymond
supporting information, p. 1664 - 1669 (2015/05/27)
Derivatives of 2-(2′-hydroxy-5′-dimethylaminobenzyl)-4,6-dimethylamino-1,3,5-triazine were synthesized by an original multistep protocol that afforded, after quaternization of the N,N-dimethylaminobenzyl moiety, water-soluble fluorescent dyes. These fluor
Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to arylmethylene cyanoacetates
Soegel, Sebastian,Tokunaga, Norihito,Sasaki, Keigo,Okamoto, Kazuhiro,Hayashi, Tamio
, p. 589 - 592 (2008/04/12)
Asymmetric 1,4-addition of arylboronic acids to (￡)-methyl 2-cyano-3-arylpropenoates proceeded in the presence of a rhodium catalyst (3 mol %) coordinated with a chiral diene ligand, (R,R)-Ph-bod*, to give high yields of the corresponding methyl 3,3-diaryl-2-cyanopropanoates with high enantioselectivity (up to 99% ee). This catalytic asymmetric transformation was applied to the asymmetric synthesis of (R)-tolterodine. American Chemical Society.
