859851-01-7 Usage
General Description
2,3-Dihydrothieno[3,4-b][1,4]dioxin-5-ylmethanol is a chemical compound with the molecular formula C9H8O3S. It is a thieno ring-fused dioxin derivative and contains a hydroxymethyl group attached to the thieno ring. This chemical is used in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceutical compounds. It has also been studied for its potential biological activities and therapeutic applications. Additionally, 2,3-dihydrothieno[3,4-b][1,4]dioxin-5-ylmethanol may also have environmental and toxicological implications that warrant further investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 859851-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,9,8,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 859851-01:
(8*8)+(7*5)+(6*9)+(5*8)+(4*5)+(3*1)+(2*0)+(1*1)=217
217 % 10 = 7
So 859851-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3S/c8-3-6-7-5(4-11-6)9-1-2-10-7/h4,8H,1-3H2
859851-01-7Relevant articles and documents
Metal-free, visible-light photoredox catalysis: Transformation of arylmethyl bromides to alcohols and aldehydes
Li, Jian,Wang, Hongni,Liu, Li,Sun, Jiangtao
, p. 49974 - 49978 (2014/12/10)
A mild, simple, and controllable metal-free photocatalytic system for the transformation of arylmethyl bromides to corresponding alcohols and aldehydes in high yields with visible-light irradiation has been achieved. Eosin Y was found to be an efficient promoter for this oxidative dehalogenation reaction under photo irradiation conditions.
Phenyl-EDOTn derivatives as super acid labile carboxylic acid protecting groups for peptide synthesis
Isidro-Llobet, Albert,álvarez, Mercedes,Albericio, Fernando
, p. 3304 - 3307 (2008/09/21)
A series of new 3,4-ethylenedioxy-2-thenyl (EDOTn) derived alcohols have been synthesized and evaluated as super acid labile carboxylic acid protecting groups. All the derivatives are labile to very low concentrations of TFA (0.01-0.5%).
