85825-85-0 Usage
General Description
2-[(4-Methylbenzyl)oxy]benzaldehyde is a chemical compound with the molecular formula C15H14O2. It is an aromatic aldehyde that contains a benzene ring and a methyl group attached to a benzyl group, which in turn is attached to an alkoxy group. 2-[(4-METHYLBENZYL)OXY]BENZALDEHYDE is used in the synthesis of various organic molecules and is commonly used as a building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It has a distinct odor and is typically handled and stored under controlled conditions due to its potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 85825-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,2 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85825-85:
(7*8)+(6*5)+(5*8)+(4*2)+(3*5)+(2*8)+(1*5)=170
170 % 10 = 0
So 85825-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c1-12-6-8-13(9-7-12)11-17-15-5-3-2-4-14(15)10-16/h2-10H,11H2,1H3
85825-85-0Relevant articles and documents
Copper-Catalyzed Asymmetric Diyne Cyclization via [1,2]-Stevens-Type Rearrangement for the Synthesis of Chiral Chromeno[3,4-c]pyrroles
Hong, Feng-Lin,Hong, Pan,Lu, Xin,Shi, Chong-Yang,Ye, Long-Wu,Zhai, Tong-Yi,Zhu, Xin-Qi
supporting information, (2021/12/27)
Here, we report a copper-catalyzed asymmetric cascade cyclization/[1,2]-Stevens-type rearrangement via a non-diazo approach, leading to the practical and atom-economic assembly of various valuable chiral chromeno[3,4-c]pyrroles bearing a quaternary carbon
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
