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2-Bromo-1,1-dimethoxyethane (Bromoacetaldehyde dimethyl acetal) was used in the synthesis of 2,3-O-acetal via reaction with 2,3-diol in the presence of 10-camphorsulphonic acid (CSA). 2-bromo-1,1-dimethoxyethane was used to react with 4-hydroxylbenzaldehyde, and finally aldehyde substituted prodrug was generated by TFA-mediated deacetalization.
Zunyi Yanga,; Hongzhi Caoa,; Jie Hua,; Renli Shanb;, Biao Yua. 1?2 Migration and concurrent glycosidation of phenyl 1-thio-α-mannopyranosides via 2, 3-O-cyclic dioxonium intermediates.. Tetrahedron. 2003, 59 (2), 249-254.
Chunyan Bao,; Ming Jin,; Bo Li,; Yaodong Xu,; Jingyan Jin,; Linyong Zhu. Long conjugated 2-nitrobenzyl derivative caged anticancer prodrugs with visible light regulated release: preparation and functionalizations. title . Org. Biomol. Chem.. 2012, 10 (27), 5238-5244.
Dichiarazioni di rischio (UE): H226-H301-H330-H315-H319-H335
Flammable liquid and vapour. Toxic if swallowed. Fatal if inhaled. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Dichiarazioni precauzionali: P260-P201-P280h-P304+P340-P405-P501a
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves/clothing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.