Interesting facts
Interesting Facts about 2-Cyanoacetohydrazide
2-Cyanoacetohydrazide is a fascinating compound widely studied in the field of organic chemistry. Here are some intriguing points about this unique chemical:
- Synthesis: This compound can be synthesized through the reaction of cyanoacetic acid with hydrazine, leading to the formation of a hydrazide structure. The versatility of such synthesis routes makes it an attractive target for organic chemists.
- Biological Activity: 2-Cyanoacetohydrazide has shown potential in biological applications, particularly in the area of antimicrobial and antitubercular activity. Research is ongoing to explore its efficacy as a therapeutic agent.
- Applications: Beyond its biological significance, this compound is also utilized in various industrial applications, such as agriculture and pharmaceuticals. It serves as an intermediate in the synthesis of more complex molecules.
- Reactivity: The presence of both a cyano group and hydrazide functional group increases its reactivity and offers unique opportunities for further modification, allowing for the creation of numerous derivatives.
- Research Interest: The compound is a subject of interest in synthetic methodology, particularly in the development of new reactions and green chemistry practices aimed at reducing environmental impacts in chemical synthesis.
2-Cyanoacetohydrazide exemplifies the beauty of chemistry, showcasing how a simple structural modification can lead to significant biological and industrial applications. Its diverse reactivity not only holds promise for innovative research but also enriches our understanding of compound interactions.
Synonyms
Cyanoacetohydrazide
2-Cyanoacetohydrazide
140-87-4
Cyacetacide
Cyacetazide
Cyanoacetic acid hydrazide
Cyanoacethydrazide
Cyacetacid
Cyacetazid
Mackreazid
Neohydrazid
Armazal
Cianazil
Cyanazide
Cyanizide
Cyazide
Dictycide
Dictyzide
Hidacian
Hidaciann
Leandin
Reazide
Tsiazid
Cyazid
Helmox
Reacid
Reazid
Cyanoethydrazide
Cyanacethydrazide
Cyanacetohydrazide
ACETIC ACID, CYANO-, HYDRAZIDE
Cyanacetylhydrazide
Cyanoacetylhydrazide
Ciacetacida
Malonitrile hydrazide
(Cyanoacetyl)hydrazine
Usaf kf-18
Malononitrile hydrazide
Cyacetacide [INN]
Cyanoacetic hydrazide
Cyanoacetyl hydrazide
Cyacetacidum
Kyanacethydrazid
Cyanacetic acid hydrazide
Cyacetacidum [INN-Latin]
Ciacetacida [INN-Spanish]
AB-42
HSDB 2701
Cyacetacide [INN:BAN]
Cyanacetic acid, hydrazide
EINECS 205-437-2
Cyanoacetylhydrazine
NSC 24261
NSC-24261
2-Cyanoacethydrazide
UNII-40H59YCS67
BRN 1751498
2-Cyanoacetylhydrazide
DTXSID9046572
AI3-23466
CYACETACIDE [MI]
CYACETACIDE [HSDB]
.alpha.-Cyanoacetohydrazide
CYACETACIDE [MART.]
(.alpha.-Cyanoacetyl)hydrazine
DTXCID7026572
Alpha-cyanoacetic acid, hydrazide
40H59YCS67
4-02-00-01895 (Beilstein Handbook Reference)
NCGC00166240-01
Cyanacethydrazine
Cyacetacidum (INN-Latin)
Ciacetacida (INN-Spanish)
CYACETACIDE (MART.)
Cyazide (VAN)
Kyanacethydrazid [Czech]
USAF kf-28
methane, C-cyano-C-hydrazinocarbonyl-
CAS-140-87-4
MFCD00007611
DIETYCIDE
cyanoacetic acid hydrazone
acetohydrazide, 2-cyano-
WLN: ZMV1CN
Cyanoacetohydrazide, 98%
Cyanoacetic acid, hydrazide
(alpha-Cyanoacetyl)hydrazine
alpha-cyanoacetic acid hydrazide
CHEMBL2106008
Acetic acid, 2-cyano-, hydrazide
HY-B0994
NSC24261
Tox21_112366
BBL010619
STK298870
AKOS000119759
Tox21_112366_1
CCG-213834
CS-4488
NCGC00166240-02
FC164964
DB-042536
NS00024567
EN300-19656
AB00442940_02
12B-129
AC-907/25014397
SR-01000944252
SR-01000944252-1
BRD-K39371216-001-01-3
Q27258330
F2111-0015
Z104474618
205-437-2
Solubility of 2-Cyanoacetohydrazide
2-Cyanoacetohydrazide, a chemical compound with the formula C4H6N4O, exhibits some interesting solubility characteristics that are worth noting. Understanding its solubility can be crucial for various applications in chemical synthesis and research.
Solubility Profile
Regarding solubility, 2-cyanoacetohydrazide tends to be:
Furthermore, it is crucial to note that:
In summary, the solubility of 2-cyanoacetohydrazide in various solvents emphasizes its behavior as a polar compound, which is essential for its usage in many chemical applications. As one might conclude, “the solubility of a compound often dictates its chemical behavior and potential for reactions."