HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
Huagongshe Open Program:[email protected]AI access: llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.7.9
  1. Home
  2. /Compound

N-(4-(5-Nitro-2-furyl)-2-thiazolyl)formamide

HCID 32486
New noteNew reactionRequest quotesPrint preview
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
24554-26-5
Standard SMILES
O=CNc1nc(-c2ccc([N+](=O)[O-])o2)cs1
InChIKey
ZQBWQLJJMGJREB-UHFFFAOYSA-N
Molecular formula
C8H5N3O4S
Average molar mass
239.21 g/mol
Monoisotopic mass
239.00007682

Overview

N-(4-(5-nitro-2-furyl)thiazoyl)formamide appears as dark yellow powder or gold solid. (NTP, 1992)

Names & identifiers

Preferred name
N-(4-(5-Nitro-2-furyl)-2-thiazolyl)formamide
IUPAC
N-[4-(5-nitrofuran-2-yl)-1,3-thiazol-2-yl]formamide
English name
N-[4-(5-Nitro-2-furyl)-2-thiazolyl]formamide.
Molecular formula
C8H5N3O4S
Molecular weight
239.21

Names & synonyms

FANFT24554-26-5N-(4-(5-Nitro-2-furyl)-2-thiazolyl)formamideN-[4-(5-Nitro-2-furyl)-2-thiazolyl]formamide2-Formylamino-4-(5-nitro-2-furyl)thiazole7N99PZG62ODTXSID4020953Formamide, N-(4-(5-nitro-2-furanyl)-2-thiazolyl)-NSC-155010Formamide, N-(4-(5-nitro-2-furyl)-2-thiazolyl)-Formamide, N-[4-(5-nitro-2-furanyl)-2-thiazolyl]-Formamide, N-[4-(5-nitro-2-furyl)-2-thiazolyl]-
Show more names
N-(4-(NITRO-2-FURYL)-THIAZOLYL)-FORMAMIDEN-(4-(5-NITRO-2-FURYL)-THIAZOLYL-FORMAMIDEN-(N-(5-NITRO-2-FURYL)-2-THIAZOLYL)FORMAMIDEN-[4-(5-Nitro-2-furyl)-2-thiazolyl]formamide.N-(4-(5-NITRO-2-FURANYL)-2-THIAZOLYL)-FORMAMIDE
RefChem:139928N-4-(5-Nitro-2-furyl)-2-thiazolylformamideDTXCID80953N-[4-(5-nitrofuran-2-yl)-1,3-thiazol-2-yl]formamideNSC 155010N-(4-(5-nitrofuran-2-yl)thiazol-2-yl)formamideN-(4-(5-Nitro-2-furyl)-2-thiazolyl)formamidN-((4-(5-Nitro-2-furyl)-2-tiazolyl))formamide

Database identifiers

Properties

Computed structural properties

XLogP
1.4
Topological polar surface area
129 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
6
Rotatable bonds
2
Heavy atoms
16
Formal charge
0
Complexity
285

Experimental & physicochemical properties

Solubilityless than 1 mg/mL at 70 °F (NTP, 1992)
Melting Point549.5 to 562.1 °F (NTP, 1992)
Physical DescriptionN-(4-(5-nitro-2-furyl)thiazoyl)formamide appears as dark yellow powder or gold solid. (NTP, 1992)

Physicochemical properties

Boiling point
200 °C · 200°C (rough estimate)
Density
1.6331 · 1.6331 (rough estimate)
refractive index
1.632 · 1.6320 (estimate)
CAS DataBase Reference
24554 · 24554-26-5
FDA UNII
7 N99PZG62O · 7N99PZG62O
EPA Substance Registry System
N-[(4-(5-Nitro-2-furyl)-2-tiazolyl)]formamide (24554-26-5)

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Hazard information

Fire HazardsFlash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
Health HazardsACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits very toxic fumes of sulfur oxides and nitrogen oxides. (NTP, 1992)
Reactive GroupAmides and Imides
Reactivity Profile · 1 item

A nitrated organosulfide and amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Air and Water ReactionsInsoluble in water.

Safety & protection

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 item

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Chemistry & industry

Applications

General DescriptionDark yellow powder or gold solid.

Suppliers

Loading…

Open inquiries

Loading…

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
CAS
24554-26-5
PubChem CID
32486
DTXSID
DTXSID4020953
ChEMBL
CHEMBL82444
UNII
7N99PZG62O
Nikkaji
J1.005G
Nonfire Spill Response · 1 item

SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Personal Protective Equipment (PPE) · 1 item

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)