6-Methoxypyridine-2-boronicacidN-phenyldiethanolamineester
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6-Methoxypyridine-2-boronicacidN-phenyldiethanolamineester
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CAS No:
872054-59-6
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Formula:
C16H19BN2O3
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Chemical Name:
6-Methoxypyridine-2-boronicacidN-phenyldiethanolamineester
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Synonyms:
6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester;2-{1-oxa-4-azaspiro[4.5]deca-6,8-dien-4-yl}ethan-1-ol;6-Methyl-2-pyridineboronic acid N-phenyldiethanolamine ester, 6-Methyl-2-pyridineboronic acid[2,2-(phenylimino)diethanol]ester
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CAS No:
6-Methoxypyridine-2-boronicacidN-phenyldiethanolamineester Basic Attributes
298.15
298.1488726
DTXSID90584607
Safety Information
UN 3175 4.1/PG 2
3
36/37/38-67-41-37/38
26-36-39
Xi
|Warning|H228 (100%): Flammable solid [Danger Flammable solids]|P210, P240, P241, P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
6-Methoxypyridine-2-boronicacidN-phenyldiethanolamineester Use and Manufacturing
Reactant for:• ;Preparation of alkylated sulfonamides via alkylation with alcohols catalyzed by Ag/Mo hybrid1• ;Preparation of 7-disubstituted oxyindoles as EP3 receptor antagonists2• ;Preparation of N-substituted sulfonamides via ferrous chloride-catalyzed N-alkylation with benzylic alcohols3• ;Preparation of (alkyl)hydroxybenzimidazoles, via a O- to N-acyl transfer reaction, as intermediates for EP3 receptor antagonists4• ;Preparation of N-arylsulfonyl β-[(aryloxy)indolyl]acrylamides as potent and selective EP3 receptor antagonists5
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