13826-12-5 Usage
Chemical compound
Benzenemethanol, 3-[4-(hydroxymethyl)phenoxy]-
Structure
Consists of a benzene ring with a hydroxymethyl group attached to a phenoxy group at the 3-position on the benzene ring.
Versatile compound
Potential applications in organic synthesis, pharmaceuticals, and materials science.
Reactivity
Hydroxymethyl group provides reactivity for further functionalization.
Polarity
Phenoxy group adds some polarity to the molecule.
Potential for diverse applications
Structural features offer potential for diverse applications in various industries.
Further research and development
May lead to new uses and potential benefits in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13826-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,2 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13826-12:
(7*1)+(6*3)+(5*8)+(4*2)+(3*6)+(2*1)+(1*2)=95
95 % 10 = 5
So 13826-12-5 is a valid CAS Registry Number.
13826-12-5Relevant academic research and scientific papers
Steps towards a practical synthesis of macrocyclic bisbenzylisoquinolines
Al-Hiari, Yusuf M.,Bennett, Stephen J.,Cox, Brian,Davies, Robert J.,Khalaf, Abedawn I.,Waigh, Roger D.,Worsley, Alan J.
, p. 647 - 659 (2007/10/03)
There are more than 400-reported bisbenzylisoquinoline alkaloids, many with interesting biological activity, but the reported syntheses are long and low yielding. As a result, there have been no systematic attempts at exploitation of the potential therapeutic applications. The concept of a sulfur 'stitch', restricting the conformational freedom of intermediates in the synthesis, will potentially allow analogues of the natural products to be prepared using relatively efficient routes. The synthesis of intermediate sulfur heterocycles is reported, based on 2,8-dimethylphenoxathiin, leading via 2,8-bis(bromomethyl) phenoxathiin-10,10-dioxide to a synthesis of 3,4,8,9-tetrahydro-13-oxa-6-thia-2, 10-diazapentacene, a key potential intermediate on the route to a variety of macrocyclic bisbenzylisoquinolines.
