Interesting facts
Interesting Facts about Pyridine-4-Carbohydrazide
Pyridine-4-carbohydrazide is a fascinating compound with a variety of applications and properties that make it noteworthy in the field of chemistry.
1. Structure and Characteristics
This compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of the hydrazide functional group enhances its reactivity and potential utilizations. The unique structure allows for various chemical behaviors, making it a versatile molecule in organic synthesis.
2. Synthetic Importance
Pyridine-4-carbohydrazide serves as a valuable intermediate in organic chemistry. Its derivatives have found applications in:
- Pharmaceuticals: Serving as an essential building block for drug synthesis.
- Agriculture: Utilized in the development of agrochemicals.
- Materials Science: Exploring its properties for creating novel materials.
3. Biological Activity
Research has indicated that this compound and its derivatives can exhibit interesting biological activities. Some studies have shown:
- Antimicrobial Properties: They may inhibit the growth of certain bacteria and fungi.
- Anti-inflammatory Effects: Potential use in treatments related to inflammatory conditions.
- Possible Anticancer Activities: Ongoing research is investigating their role in cancer therapeutics.
4. Versatility in Chemical Reactions
Pyridine-4-carbohydrazide can participate in numerous chemical reactions, including:
- Hydrazone Formation: Reacting with aldehydes or ketones to form hydrazones.
- Condensation Reactions: Being involved in the synthesis of more complex molecules.
- Electrophilic Substitution: Where it can act as a nucleophile due to the electron-rich nature of the pyridine ring.
5. Research and Development
The study of pyridine-4-carbohydrazide continues to evolve, with ongoing investigations revealing exciting new properties and applications. As a chemist or student, one might say:
“Understanding the subtle nuances of such compounds can unlock doors to innovative scientific advancements.”
In summary, pyridine-4-carbohydrazide is much more than just a chemical compound; it is a gateway to numerous opportunities in synthesis, pharmaceuticals, and materials science. Its diverse properties make it a subject of interest for chemists striving to develop new technologies and solutions.
Synonyms
isoniazid
54-85-3
Isonicotinic acid hydrazide
Isonicotinohydrazide
pyridine-4-carbohydrazide
Isoniazide
Rimifon
Nydrazid
Cotinazin
Hydrazid
Iscotin
Mybasan
Isonicotinylhydrazine
Atcotibine
Hidrasonil
Isobicina
Isonicotan
Neumandin
Armazid
Armazide
Dinacrin
Ditubin
Eralon
Ertuban
Isidrina
Laniazid
Cedin
Hyzyd
Isonicotinic hydrazide
Andrazide
Neoteben
Nicizina
Niconyl
Nicotibina
Nicozide
Pycazide
Stanozide
Isolyn
Isohydrazide
Isonicotinhydrazid
Antimicina
Chemiazid
Chemidon
Fimalene
Hidranizil
Hidrulta
Ismazide
Isocidene
Isocotin
Isonerit
Isonicid
Isonicotil
Isonidrin
Isonikazid
Isonilex
Isonindon
Isonirit
Isoniton
Isonizide
Isotebezid
Nidrazid
Nyscozid
Pyricidin
Pyrizidin
Raumanon
Retozide
Rimitsid
Teebaconin
Tubazide
Azuren
Cemidon
Defonin
Diforin
Ebidene
Eutizon
Evalon
Hidrun
Hycozid
Idrazil
Inizid
Isocid
Isonex
Isonico
Isonide
Isonin
Isozide
Isozyd
Neoxin
Niadrin
Nicetal
Nidaton
Nikozid
Niplen
Nitadon
Pelazid
Rimicid
Tubazid
Antituberkulosum
Nevin
Inah
Ido-tebin
Isoniacid
Nicotibine
Nicotisan
Rimiphone
Tisiodrazida
Tubilysin
Isotebe
Isotinyl
Nicazide
Phthisen
Pyreazid
4-Pyridinecarboxylic acid, hydrazide
Percin
Razide
Tyvid
Neo-Tizide
Isoniazid SA
Armacide
Cortinazine
Cotinizin
GINK
Isonicazide
Isotamine
Robisellin
Sauterazid
Tibinide
Unicozyde
Vazadrine
Zonazide
Dibutin
Hyozid
Isonicotinyl hydrazide
Tebecid
Tekazin
Tubeco
Tubicon
Tubomel
Vederon
Zinadon
Isonicotinoyl hydrazide
Dow-Isoniazid
4-Pyridinecarboxylic acid hydrazide
Preparation 6424
TB-Razide
Sanohidrazina
Laniozid
Pyridicin
Robiselin
Sauterzid
Tibazide
Tibizide
Tuberian
Unicocyde
Niteban
Roxifen
Tebenic
Tebexin
Tebilon
Tibison
Tibivis
Tibusan
Tizide
Tebos
Tisin
Inh-Burgthal
TB-Vis
FSR 3
TB-Phlogin
Isoniazida
Isoniazidum
Tubizid
Zidafimia
Isozid
INH
Nitebannsc 9659
In-73
Cedin (Aerosol)
RU-EF-Tb
bacillen
tebemid
tubercid
Isonizida
Isokin
Tibemid
Isonicotinoylhydrazine
4-Pyridinecarbonylhydrazine
Isonicotinsaeurehydrazid
FSR-3
4-(Hydrazinocarbonyl)pyridine
BP 5015
4-Pyridylcarbonylhydrazide
isonicotinoylhydrazide
Dianicotyl
Ipcazide
NSC 9659
4-pyridinecarbohydrazide
4-Pyridinecarboxylic hydrazide
RP-5015
Isonicotinylhydrazide
Usaf cb-2
HIA
Isonicotinyl hydrazine
pyridine-4-carboxylic acid hydrazide
CCRIS 351
MFCD00006426
CHEBI:6030
5015 RP
L 1945
HSDB 1647
Isoniazidum [INN-Latin]
Isoniazida [INN-Spanish]
5015 R.P.
UNII-V83O1VOZ8L
NSC-9659
EINECS 200-214-6
V83O1VOZ8L
RP 5015
I.A.I.
DTXSID8020755
isonicotinate hydrazide
Idrazide dell'acido isonicotinico
AI3-23936
NSC9659
CHEMBL64
DTXCID20755
MLS000069444
Isoniazid [USP:INN:BAN:JAN]
RIFATER COMPONENT ISONIAZID
RIFAMATE COMPONENT ISONIAZID
CAS-54-85-3
NCGC00016244-09
Continazine
Tubecotubercid
Abdizide
Anidrasona
SMR000059082
Tibiazide
Fetefu
Hydra
Isoniazidum (INN-Latin)
Isoniazida (INN-Spanish)
ISONIAZID (MART.)
ISONIAZID [MART.]
ISONIAZID (USP-RS)
ISONIAZID [USP-RS]
LANIZID
ISONIAZID (EP IMPURITY)
ISONIAZID [EP IMPURITY]
ISONIAZID (EP MONOGRAPH)
ISONIAZID [EP MONOGRAPH]
ISONIAZID (USP MONOGRAPH)
Isoniazid (USP:INN:BAN:JAN)
ISONIAZID [USP MONOGRAPH]
RY-EF-Tb
[(4-Pyridinylcarbonyl)oxy]hydrazine
Isoniazid; pyridine-4-carbohydrazide
AZT + Isoniazid
FRS-3
Isoniazid & EEP
Laniazid (TN)
ISONICOTINIC ACID HYDRAZIDE (IARC)
ISONICOTINIC ACID HYDRAZIDE [IARC]
((4-PYRIDINYLCARBONYL)OXY)HYDRAZINE
Isoniazid & Propolis
Isonicotinsaeurehydrazid [German]
INHd20
SR-01000003025
lsoniazid
Hydrazide, Isonicotinic Acid
Mayambutol
Dinocrin
Idrazide dell'acido isonicotinico [Italian]
isoniazid (inh)
isonicotinhydrazide
Soniazid,(S)
NIZ
Prestwick_578
Isoniazid (Tubizid)
Isoniazid 300 mg
Isoniazid(Tubizid)?
ISOZIN
Isoniazid (Standard)
Rifater (Salt/Mix)
Isonicotinsaurehydrazid
Isonicotinic acid hydrazide (Isoniazid)
Isonicotinicacidhydrazide
Spectrum_000853
ISONIAZID [INN]
ISONIAZID [JAN]
Opera_ID_454
ISONIAZID [MI]
isonicotinicacid hydrazide
ISONIAZID [HSDB]
isonicotinic acid hydrazid
Prestwick0_000161
Prestwick1_000161
Prestwick2_000161
Prestwick3_000161
Spectrum2_000107
Spectrum3_000472
Spectrum4_000022
Spectrum5_000876
ISONIAZID [VANDF]
T.B. RAZIDE
I0138
WLN: T6NJ DVMZ
isonicotinic acid hydrazone
SCHEMBL228
Biomol-NT_000288
Epitope ID:141801
4-Pyridylcarbonyl hydrazide
ISONIAZID [WHO-DD]
ISONIAZID [WHO-IP]
Oprea1_396155
BSPBio_000021
BSPBio_002204
KBioGR_000423
KBioSS_001333
MLS001055327
BIDD:GT0140
DivK1c_000070
SPECTRUM1500355
SPBio_000094
SPBio_001942
Isoniazid (JP18/USP/INN)
pyridine, 4-hydrazinocarbonyl-
BPBio1_000025
BPBio1_001322
SCHEMBL2998929
ISONIAZID [ORANGE BOOK]
component of Niadox (Salt/Mix)
GTPL12761
HMS500D12
HY-B0329R
KBio1_000070
KBio2_001333
KBio2_003901
KBio2_006469
KBio3_001424
NINDS_000070
4-Pyridinecarboxamide, 2'-amino-
HMS1568B03
HMS1920H09
HMS2089I16
HMS2091N19
HMS2095B03
HMS2234G04
HMS3259E19
HMS3373O01
HMS3655L03
HMS3712B03
KUC109571N
Pharmakon1600-01500355
4-pyridinecarbohydrazide(Isoniazid)
ISONIAZIDUM [WHO-IP LATIN]
BCP13791
HY-B0329
STR00210
Anti-TNF monoclonal antibody & INH
Tox21_113640
Tox21_201367
Tox21_300193
BBL008409
BDBM50336507
CCG-39710
NSC757078
s1937
STK086288
ISONIAZID COMPONENT OF RIFATER
(HBD) Human beta-defensin-1 & INH
AKOS000119062
ISONIAZID COMPONENT OF RIFAMATE
Isonicotinic acid hydrazide(Isoniazid)
Tox21_113640_1
AI24685
DB00951
KSC-27-048
NC00513
NSC-757078
PS-4129
IDI1_000070
UPCMLD0ENAT5791176:001
NCGC00016244-01
NCGC00016244-02
NCGC00016244-03
NCGC00016244-04
NCGC00016244-05
NCGC00016244-06
NCGC00016244-07
NCGC00016244-08
NCGC00016244-10
NCGC00016244-11
NCGC00016244-12
NCGC00016244-14
NCGC00016244-15
NCGC00016244-17
NCGC00022648-03
NCGC00022648-04
NCGC00022648-05
NCGC00022648-06
NCGC00022648-07
NCGC00254094-01
NCGC00258919-01
SY010614
Isoniazid, Vetec(TM) reagent grade, 98%
SBI-0051419.P003
AB00052025
ISONICOTINIC ACID HYDRAZIDE [WHO-IP]
NS00006598
SW196752-3
EN300-18498
ISONICOTINIC ACID HYDRAZIDE(ISONIAZIDE)
C07054
D00346
D70582
Isoniazid, analytical standard, >=99% (TLC)
AB00052025-20
AB00052025-21
AB00052025_22
AB00052025_23
AB00052025_24
AB00052025_25
AE-641/02310003
Q423169
4-PYRIDINECARBOXYLIC ACID HYDRAZIDE [WHO-IP]
SR-01000003025-2
SR-01000003025-3
BRD-K87202646-001-26-8
BRD-K87202646-001-32-6
BRD-K87202646-001-33-4
BRD-K87202646-061-04-9
BRD-K87202646-061-05-6
Isoniazid, certified reference material, TraceCERT(R)
Z58981801
F0391-0007
Isoniazid, European Pharmacopoeia (EP) Reference Standard
Isoniazid, United States Pharmacopeia (USP) Reference Standard
4-Pyridinecarboxylic acid hydrazide;Isonicotinic acid hydrazide;4-(Hydrazinocarbonyl)pyridine
InChI=1/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10
Isoniazid, Pharmaceutical??Secondary??Standard;??Certified??Reference??Material
200-214-6
Solubility of Pyridine-4-Carbohydrazide
Pyridine-4-carbohydrazide (C6H7N3O) exhibits interesting solubility characteristics that are primarily influenced by its functional groups and overall molecular structure. Here are some key points regarding its solubility:
In summary, the solubility of pyridine-4-carbohydrazide plays a crucial role in its applications in chemical processes and analytical methods, making it a compound of interest in numerous scientific fields.