Autonomic nervous system drugs

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is used as a ntrogen source for syntheis of many heterocyclic compounds and is also used as a

Formula: C194H295N53O58S Formula weight: 4329.79 Harmonized Tariff Code:  2933.29

Formula: C203H311N55O60S Formula weight: 4514.03 Harmonized Tariff Code:  2933.29

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Anisole can be obtained from the reaction between methyl formate and sodium phenolate or potassium phenolate at high temperature and pressure. Application Anisole has been used as a dopant to improve the sensitivity of photoionization at

Anisole can be obtained from the reaction between methyl formate and sodium phenolate or potassium phenolate at high temperature and pressure. Application Anisole has been used as a dopant to improve the sensitivity of photoionization at

Anisole can be obtained from the reaction between methyl formate and sodium phenolate or potassium phenolate at high temperature and pressure. Application Anisole has been used as a dopant to improve the sensitivity of photoionization at

Anisole can be obtained from the reaction between methyl formate and sodium phenolate or potassium phenolate at high temperature and pressure. Application Anisole has been used as a dopant to improve the sensitivity of photoionization at

Application Anisole may undergo: Zeolite-catalyzed Friedel-Crafts acylation with acetic anhydride in acetic acid to form 4-methoxyacetophenone with high selectivity. Bismuth triflate-catalyzed Friedel-Crafts benzoylation with benzoic anhydride to

Application Anisole may undergo: Zeolite-catalyzed Friedel-Crafts acylation with acetic anhydride in acetic acid to form 4-methoxyacetophenone with high selectivity. Bismuth triflate-catalyzed Friedel-Crafts benzoylation with benzoic anhydride to

Application Anisole may undergo: Zeolite-catalyzed Friedel-Crafts acylation with acetic anhydride in acetic acid to form 4-methoxyacetophenone with high selectivity. Bismuth triflate-catalyzed Friedel-Crafts benzoylation with benzoic anhydride to