4-Chloro-3-sulfamoylbenzoyl chloride

98%

Reagent Code: #47139
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CAS Number 70049-77-3

science Other reagents with same CAS 70049-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.0900 g/mol
Formula C₇H₅Cl₂NO₃S
badge Registry Numbers
MDL Number MFCD08063955
thermostat Physical Properties
Boiling Point 424.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.621g/cm3
Storage room temperature

description Product Description

Used primarily in the synthesis of pharmaceuticals, this compound serves as a key intermediate in the production of diuretics and antihypertensive agents. It is particularly valuable in the preparation of sulfonamide-based drugs, which are widely used to manage conditions like hypertension and edema. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive benzoyl chloride group, enabling efficient acylation reactions. Its sulfamoyl moiety also contributes to the development of bioactive compounds with potential therapeutic properties.

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inventory 5g
10-20 days ฿594.00

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4-Chloro-3-sulfamoylbenzoyl chloride
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Used primarily in the synthesis of pharmaceuticals, this compound serves as a key intermediate in the production of diuretics and antihypertensive agents. It is particularly valuable in the preparation of sulfonamide-based drugs, which are widely used to manage conditions like hypertension and edema. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive benzoyl chloride group, enabling efficient acylation reactions. Its sulfamoyl moiety also contri

Used primarily in the synthesis of pharmaceuticals, this compound serves as a key intermediate in the production of diuretics and antihypertensive agents. It is particularly valuable in the preparation of sulfonamide-based drugs, which are widely used to manage conditions like hypertension and edema. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive benzoyl chloride group, enabling efficient acylation reactions. Its sulfamoyl moiety also contributes to the development of bioactive compounds with potential therapeutic properties.

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