447409-55-4 Usage
Uses
Used in Flavoring and Fragrance Industry:
2-[(2-METHYLBENZYL)OXY]BENZALDEHYDE is used as a flavoring agent and fragrance ingredient for its aromatic properties, enhancing the sensory experience of various consumer products and personal care items.
Used in Perfumery:
In the perfumery industry, 2-[(2-METHYLBENZYL)OXY]BENZALDEHYDE is used as a key component in the creation of perfumes, contributing to their unique and appealing scents.
Used in Soap and Cosmetics Production:
2-[(2-METHYLBENZYL)OXY]BENZALDEHYDE is also utilized in the formulation of soaps and cosmetics, where it imparts pleasant odors and enriches the overall product quality.
Used in Organic Synthesis:
2-[(2-METHYLBENZYL)OXY]BENZALDEHYDE is used as a building block in the synthesis of other organic compounds, indicating its versatility in chemical manufacturing processes.
Used in Pharmaceutical Industry:
With potential applications in the pharmaceutical sector, 2-[(2-METHYLBENZYL)OXY]BENZALDEHYDE may be employed in the development of new drugs, although further research and development are required to explore its full potential in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 447409-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,7,4,0 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 447409-55:
(8*4)+(7*4)+(6*7)+(5*4)+(4*0)+(3*9)+(2*5)+(1*5)=164
164 % 10 = 4
So 447409-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c1-12-6-2-3-8-14(12)11-17-15-9-5-4-7-13(15)10-16/h2-10H,11H2,1H3
447409-55-4Relevant academic research and scientific papers
Potassium tert-Butoxide-Mediated Condensation Cascade Reaction: Transition Metal-Free Synthesis of Multisubstituted Aryl Indoles and Benzofurans
Yang, Pengfei,Xu, Weiyan,Wang, Rongchao,Zhang, Min,Xie, Chunsong,Zeng, Xiaofei,Wang, Min
supporting information, p. 3658 - 3662 (2019/05/17)
An efficient and facile method to synthesize valuable disubstituted 2-aryl indoles and benzofurans in good yields has been demonstrated, based on a tert-butoxide-mediated condensation reaction involving a vinyl sulfoxide intermediate. Products are obtained from N- or O-benzyl benzaldehydes using dimethyl sulfoxide as a carbon source. The methodology features a wide functional group tolerance and transition metal-free environment. Preliminary mechanistic studies suggest that the reaction involves a tandem aldol reaction/Michael addition/dehydrosulfenylation/isomerization sequence through an ionic protocol.
Neighboring lithium-assisted [1,2]-wittig rearrangement: Practical access to diarylmethanol-based 1,4-diols and optically active binol derivatives with axial and sp3-central chirality
Gao, Guang,Gua, Feng-Lei,Jiang, Jian-Xiong,Jiang, Kezhi,Sheng, Chun-Qi,Lai, Guo-Qiao,Xu, Li-Wen
scheme or table, p. 2698 - 2703 (2011/04/15)
A facile and practical methodology for the synthesis of synthetically useful diarylmethanol-based 1,4-diols and enantiomerically pure BINOL-derived diols with axial and sp3-central chirality has been developed through neighboring lithium-promot
