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N-formamidoformamide

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Identification
Molecular formula
C2H4N2O2
CAS number
7553-62-4
IUPAC name
N-formamidoformamide
State
State

At room temperature, N-formamidoformamide is a liquid.

Melting point (Celsius)
3.00
Melting point (Kelvin)
276.20
Boiling point (Celsius)
182.50
Boiling point (Kelvin)
455.70
General information
Molecular weight
74.08g/mol
Molar mass
74.0800g/mol
Density
1.3230g/cm3
Appearence

N-formamidoformamide is a colorless liquid with a pungent odor.

Comment on solubility

Solubility of N-formamidoformamide

N-formamidoformamide, with the chemical formula N-H2COH2(H2NCOH), is an intriguing compound when it comes to solubility. Its unique chemical structure contributes to its behavior in various solvents.

Solubility Characteristics:

  • Polar Solvents: N-formamidoformamide is generally soluble in polar solvents such as water due to its ability to form hydrogen bonds.
  • Non-Polar Solvents: It exhibits low solubility in non-polar solvents, limiting its use in non-aqueous environments.
  • Temperature Dependence: Solubility may increase with temperature, indicating that heating could enhance its dissolution in solvents.

In summary, the solubility of N-formamidoformamide demonstrates a clear preference for polar environments. As the old saying goes, “like dissolves like,” and this compound is a prime example of that principle in action.

Interesting facts

Interesting Facts about N-formamidoformamide

N-formamidoformamide, a fascinating compound in the realm of organic chemistry, exhibits unique properties and applications that intrigue both researchers and students alike.

Key Characteristics:

  • Structure: N-formamidoformamide is an intriguing molecule with dual formamide groups, which imparts unique reactivity and functionality.
  • Hydrogen Bonding: The presence of multiple amide groups allows for extensive hydrogen bonding, affecting both its physical properties and interactions with other molecules.
  • Synthesis: The synthesis of N-formamidoformamide can involve various methods, often showcasing the creativity of chemists in adapting existing reactions to achieve desired compounds.

Applications:

  • Research: This compound has been studied for its role in biological systems, particularly in modeling peptide bonds and interactions within protein structures.
  • Potential in Drug Design: Due to its amide functionalities, N-formamidoformamide has potential applications in pharmaceutical research, particularly in designing new therapeutics.
  • Industrial Uses: Compounds similar to N-formamidoformamide are often utilized in various industrial processes, including the synthesis of polymers and as intermediates in chemical manufacturing.

In summary, N-formamidoformamide is more than just a simple organic compound; it serves as a cornerstone for understanding complex chemical behaviors and developing innovative applications. As one researcher put it, "The beauty of chemistry lies in how simple components can combine to create intricate functionalities."
This sentiment captures the essence of what makes N-formamidoformamide a subject of interest in the chemical sciences.

Synonyms
1,2-Diformylhydrazine
628-36-4
1,2-Hydrazinedicarboxaldehyde
DIFORMYLHYDRAZINE
Bicarbamaldehyde
Diformohydrazide
N,N'-Diformylhydrazine
s-Diformohydrazide
s-Diformylhydrazine
Hydrazine, 1,2-diformyl-
Formic acid, hydrazodi-
1,2-Diformylhydrazin
NSC 54729
CCRIS 1863
Hydrazinedicarboxaldehyde
1,2-Diformylhydrazin [German]
EINECS 211-040-5
BRN 1740259
DTXSID8020468
AI3-62052
DTXCID00468
4-02-00-00086 (Beilstein Handbook Reference)
Hydrazine, 1,2-diformyl-(8CI)
povxowvflaavbh-uhfffaoysa-n
N'-formylformohydrazide
N-formamidoformamide
N'-Formylformic hydrazide
MFCD00003275
NSC-54729
Hydrazodicarbaldehyde
sym-Diformylhydrazine
diformyl hydrazine
bisformyl hydrazine
N-formamidomethanamide
sym-diformyl hydrazine
DIFORMYLHYDRAZIDE
Hydrazine,2-diformyl-
WLN: VHMMVH
RM2E8R3N3L
N'-Formylformic hydrazide #
1,2-Diformylhydrazine, 97%
CHEMBL3185965
DIFORMYLHYDRAZINE, 1,2-
ALBB-017779
NSC54729
Tox21_200133
STL553965
AKOS015915288
CS-W001208
FD66381
NCGC00248537-01
NCGC00257687-01
AS-57470
CAS-628-36-4
SY012914
DB-054302
D4595
NS00042235
EN300-157892
F14871
A834033
Q19903951