5-Nitrothiophene-2-carbonyl Chloride

95%

Reagent Code: #219510
fingerprint
CAS Number 39978-57-9

science Other reagents with same CAS 39978-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.59 g/mol
Formula C₅H₂ClNO₃S
badge Registry Numbers
MDL Number MFCD09260988
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to introduce the 5-nitrothiophene-2-carbonyl group into target molecules, enhancing their biological activity or altering solubility and stability. Commonly employed in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting inflammatory and infectious diseases. Also utilized in the preparation of functionalized polymers and specialty materials where thiophene derivatives contribute to electronic or optical properties. Its reactivity with amines and alcohols makes it valuable for constructing amide and ester linkages under controlled conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿1,870.00
inventory 1g
10-20 days ฿4,900.00
inventory 5g
10-20 days ฿21,990.00
5-Nitrothiophene-2-carbonyl Chloride
No image available

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to introduce the 5-nitrothiophene-2-carbonyl group into target molecules, enhancing their biological activity or altering solubility and stability. Commonly employed in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting inflammatory and infectious diseases. Also utilized in the preparation of functionalized p

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to introduce the 5-nitrothiophene-2-carbonyl group into target molecules, enhancing their biological activity or altering solubility and stability. Commonly employed in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting inflammatory and infectious diseases. Also utilized in the preparation of functionalized polymers and specialty materials where thiophene derivatives contribute to electronic or optical properties. Its reactivity with amines and alcohols makes it valuable for constructing amide and ester linkages under controlled conditions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...