synthesis of albendazole ppt proventil

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0000046662 00000 n Copyright © 2013-2020 MOLBASE All Rights Reserved ICP Shanghai 14014220Lead Time: synthesis ALBENDAZOLE: ALBENDAZOLE Eskazole, Zentel Methyl 5-(propylthio)-2-benzimidazole carbamate Widely employed throughout the world for the treatment of intestinal nematode function.

0000008132 00000 n x�b``�c`��a`c`P�� Ȁ �@1v�+�L� �B�cH�*�67����1Q�,;��F�M�G�j>q\��mTb�3sK�����ݵ�:i�v��N��������. 0000021464 00000 n 0000062904 00000 n 0000045750 00000 n �Į@l�������r�˖f����7�j��C�8�H3�$��n�c1 d�s�[P(�x@� �ㄿ endstream endobj 327 0 obj <>/Size 258/Type/XRef>>stream 0000008358 00000 n These are aromatic heteropolycyclic compounds that contain a carbamic acid ester group, which is N-linked to the C2-atom of a benzimidazole moiety.

H�\�͎�0�� ��3��$D�a��} Nic�Cy�uQ�Yi�>lw��v�����������l�C裿���ys�!d���C7|-�ݵ����_� 0000015430 00000 n Specifically, it relates to the process for the preparation of anti-parasite bulk drug albendazole. 0000022836 00000 n - 0000026076 00000 n

The reaction is environmental friendly, fast, and proceeds with high yield.

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0000069568 00000 n 5 Day Lead Time: 258 0 obj <> endobj xref 258 71 0000000016 00000 n 0000032577 00000 n 0000022144 00000 n 0000009540 00000 n 0000070922 00000 n 0000010335 00000 n : 54965-21-8), with other name of N-(5-Propylsulfanyl)benzimidazole-2-ylcarbamic acid methyl ester, could be produced through many synthetic methods.. 0000003414 00000 n 0000011866 00000 n

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0000008698 00000 n 0000007498 00000 n 0000003214 00000 n 0000003265 00000 n 0000004136 00000 n 0000021193 00000 n 0000018922 00000 n 0000046397 00000 n 0000019282 00000 n Albendazole, also known as albendazolum, is a medication used for the treatment of a variety of parasitic worm infestations. 0000001716 00000 n 0000011064 00000 n 0000002441 00000 n Recently, the anticancer effects of albendazole were also investigated 2,3. In this laboratory activity, students are introduced to the synthesis of an albendazole metabolite obtained by a sulfide oxidation reaction. Albendazole, also known as SK and F62979 or albenza, belongs to the class of organic compounds known as 2-benzimidazolylcarbamic acid esters. 5 Day Lead Time: 0000008837 00000 n It is useful for giardiasis, trichuriasis, filariasis, neurocysticercosis, hydatid disease, pinworm disease, and ascariasis, among other diseases It is taken by mouth. 0000013332 00000 n 0000004693 00000 n 0000015862 00000 n 0000025760 00000 n :�5ߦ�{�t�ޮ-����n6׏�.y��%����(@u���YZT��JJJj0- P��"�� �� `i&W �*�:�Z���LBo1|bZ����ɜ���/�;C(C8�P}������1���g�a���q*�T6MF_6_�/_�1La|�0���%�y%�����;�]<9��*L9���ڹ/�Ƴ�3|gl|Թ�A�����a.C%�&C5�d��L:����.S�@�p �������Q���? 0000004960 00000 n 0000025902 00000 n 0000020922 00000 n 0000014699 00000 n Keywords: Albendazole, Impurities, Synthesis, Characterization Introduction Albendazole is a broad-spectrum anthelmintics against gastrointestinal nematodes and the larval stages of cestodes 1. 0000005730 00000 n %PDF-1.4 %���� 0000063066 00000 n 1 Day Lead Time: The students synthesize albendazole metabolite 2 by oxidation of compound 1 using H 0000029370 00000 n

The oxidation reagent is H2O2 in acetic acid. 0000008671 00000 n x�bb�c`b``Ń3� �b� ܬ endstream endobj 259 0 obj <>/ViewerPreferences<>/Metadata 67 0 R/Pages 66 0 R/StructTreeRoot 69 0 R/Type/Catalog/PageLabels 64 0 R>> endobj 260 0 obj <>/ProcSet[/PDF/Text]/Properties<>/MC1<>>>/ExtGState<>>>/Type/Page>> endobj 261 0 obj [262 0 R 263 0 R 264 0 R 265 0 R] endobj 262 0 obj <>/A 309 0 R/H/N/StructParent 6/Border[0 0 0]/Type/Annot>> endobj 263 0 obj <>/A 308 0 R/H/N/StructParent 7/Border[0 0 0]/Type/Annot>> endobj 264 0 obj <>/A 307 0 R/H/N/StructParent 8/Border[0 0 0]/Type/Annot>> endobj 265 0 obj <>/A 306 0 R/H/N/StructParent 9/Border[0 0 0]/Type/Annot>> endobj 266 0 obj <> endobj 267 0 obj <>stream

0000006815 00000 n 0000003719 00000 n Albendazole as well as its metabolite, albendazole sulfoxide, are used as anthelmintic drugs. 0000002606 00000 n 0000021969 00000 n 0000017318 00000 n

0000025995 00000 n 0000071560 00000 n 7 Day Lead Time:

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