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7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

Base Information
  • Chemical Name:7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole
  • CAS No.:1268335-81-4
  • Molecular Formula:C17H19BN2O3
  • Molecular Weight:310.16
  • Hs Code.:
7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

Synonyms:7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

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Chemical Property of 7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole
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Technology Process of 7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

There total 13 articles about 7-{2'-[4''-(aminoethyl)phenylcarbamoyl]ethyl}-1,3-dihydro-1-hydroxy-2,1-benzoxaborole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
3-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-7-yl)-N-(4-((tert-butoxycarbonyl)aminomethyl)phenyl)propanamide; With hydrogenchloride; In methanol; at 20 - 25 ℃; for 6h;
With sodium hydroxide; In water;
Guidance literature:
Multi-step reaction with 10 steps
1.1: silica gel; pyridinium chlorochromate / dichloromethane / 20 - 25 °C
2.1: toluene-4-sulfonic acid / toluene / Reflux
2.2: 2 h / Reflux
3.1: sodium tetrahydroborate / methanol / 1 h / 20 - 25 °C
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 7 h / 20 - 25 °C
5.1: n-butyllithium / hexane; tetrahydrofuran / 0.33 h / -78 °C
5.2: -78 - 25 °C
6.1: sodium hydride / tetrahydrofuran; mineral oil / 20 h / 20 - 25 °C
7.1: hydrogen / platinum(IV) oxide trihydrate / methanol / 20 - 25 °C
8.1: sodium hydroxide; water / methanol / 1 h / Reflux
8.2: pH 2 / Acidic conditions
9.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0 - 25 °C
10.1: hydrogenchloride / methanol / 6 h / 20 - 25 °C
With hydrogenchloride; sodium tetrahydroborate; n-butyllithium; water; hydrogen; silica gel; sodium hydride; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; sodium hydroxide; platinum(IV) oxide trihydrate; In tetrahydrofuran; methanol; hexane; dichloromethane; toluene; mineral oil;
Guidance literature:
Multi-step reaction with 8 steps
1.1: sodium tetrahydroborate / methanol / 1 h / 20 - 25 °C
2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 7 h / 20 - 25 °C
3.1: n-butyllithium / hexane; tetrahydrofuran / 0.33 h / -78 °C
3.2: -78 - 25 °C
4.1: sodium hydride / tetrahydrofuran; mineral oil / 20 h / 20 - 25 °C
5.1: hydrogen / platinum(IV) oxide trihydrate / methanol / 20 - 25 °C
6.1: sodium hydroxide; water / methanol / 1 h / Reflux
6.2: pH 2 / Acidic conditions
7.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0 - 25 °C
8.1: hydrogenchloride / methanol / 6 h / 20 - 25 °C
With hydrogenchloride; sodium tetrahydroborate; n-butyllithium; water; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; platinum(IV) oxide trihydrate; In tetrahydrofuran; methanol; hexane; dichloromethane; mineral oil;
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