Interesting facts
Interesting Facts about 10H-phenothiazine
10H-phenothiazine is a fascinating compound that has garnered attention in various fields of research and application. Known for its unique structure, this compound features a three-ring system that contributes to its chemical properties and potential uses.
Key Highlights
- Pharmacological Significance: 10H-phenothiazine is well-known in the pharmaceutical industry, particularly as a precursor for the synthesis of numerous antipsychotic medications. Its derivatives have played a significant role in the treatment of mental health disorders.
- Diverse Applications: Beyond its medicinal use, 10H-phenothiazine has been employed in various other sectors:
- As a dye in the textile industry.
- In the preparation of pesticides and anti-fungal agents.
- In research settings for its role as a redox-active compound.
- Electron-Deficient Behavior: This compound exhibits interesting electron-deficient properties, making it useful in organic electronic applications, such as in organic solar cells and light-emitting diodes (LEDs).
- Structural Chemistry: The distinctive structure of 10H-phenothiazine allows it to participate in various chemical reactions, including oxidation and reduction processes, which are vital in synthetic organic chemistry.
Quotes
As noted by chemist Arthur F. Benner, *"The innovative applications of 10H-phenothiazine highlight the beauty of how structure influences function in chemistry."*
Conclusion
In summary, 10H-phenothiazine is not just a compound of academic interest; it bridges the gap between theoretical research and practical applications. Its diverse uses, particularly in medicine and materials science, underscore its significance in ongoing scientific exploration.
Synonyms
PHENOTHIAZINE
10H-Phenothiazine
92-84-2
Thiodiphenylamine
Dibenzothiazine
Contaverm
Dibenzo-1,4-thiazine
Fenoverm
Phenosan
Feeno
Phenthiazine
Nemazine
Agrazine
Antiverm
Fenotiazina
Fentiazin
Helmetina
Lethelmin
Nemazene
Nexarbol
Padophene
Penthazine
Phenegic
Phenoverm
Phenovis
Phenoxur
Phenzeen
Souframine
Orimon
Reconox
Thiodiphenylamin
Wurm-Thional
AFI-Tiazin
Dibenzoparathiazine
Early bird wormer
10H-Phenothiazin
Dibenzo-p-thiazine
Fenothiazine
Tiodifenilamina
Biverm
Thiodifenylamine
Phenthiazinum
Danikoropa
ENT 38
Phenothiazinum
Caswell No. 652
XL-50
Phenothiazine [INN]
phenothiazin
CCRIS 5877
EPA Pesticide Chemical Code 064501
HSDB 5279
UNII-GS9EX7QNU6
GS9EX7QNU6
Fenotiazina [INN-Spanish]
NSC 2037
NSC-2037
EINECS 202-196-5
Phenothiazinum [INN-Latin]
MFCD00005015
BRN 0143237
ENT-38
DTXSID5021126
CHEBI:37931
AI3-00038
CHEMBL828
MLS000069413
DTXCID301126
EC 202-196-5
4-27-00-01214 (Beilstein Handbook Reference)
Phenothiazine (INN)
NCGC00091146-02
NCGC00091146-04
SMR000059045
Fenotiazina (INN-Spanish)
Phenothiazinum (INN-Latin)
PHENOTHIAZINE (USP-RS)
PHENOTHIAZINE [USP-RS]
Fenothiazine [Dutch]
Fenotiazina [Italian]
Thiodifenylamine [Dutch]
Phenothiazine,C12H9NS,92-84-2
Thiodiphenylamin [German]
Tiodifenilamina [Italian]
CAS-92-84-2
Phenothiazine [INN:NF]
ALIMEMAZINE HEMITARTRATE IMPURITY C (EP IMPURITY)
ALIMEMAZINE HEMITARTRATE IMPURITY C [EP IMPURITY]
PROMETHAZINE HYDROCHLORIDE IMPURITY A (EP IMPURITY)
PROMETHAZINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Contraverm
a phenothiazine
2,3:5,6-Dibenzo-1,4-thiazine
Nemazine (veterinary)
Phenothiazine (Standard)
Phenothiazine, >=98%
Opera_ID_1719
PHENOTHIAZINE [MI]
cid_7108
SCHEMBL9114
PHENOTHIAZINE [HSDB]
Nemazine [veterinary] (TN)
Oprea1_495637
MLS001424182
MLS002152928
MLS003166904
BIDD:GT0831
PHENOTHIAZINE [WHO-DD]
Phenothiazine, SAJ first grade
SCHEMBL2395921
CHEBI:37932
CHEBI:38093
HY-Y0055R
WLN: T C666 BM ISJ
NSC2037
HMS1607G06
HMS2052I13
HMS2230N12
HMS3372C18
HMS3394I13
HMS3652J21
HMS3715J12
HMS3885P13
Pharmakon1600-01506171
PHENOTHIAZINE [GREEN BOOK]
HY-Y0055
Tox21_111090
Tox21_400010
BBL011728
BDBM50012855
NSC760392
s4251
STK205834
AKOS000119180
Tox21_111090_1
CCG-101115
DB11447
FD53774
NC00365
NSC-760392
PS-3980
PHENOTHIAZINE, REFERENCE STANDARD
NCGC00091146-01
NCGC00091146-03
NCGC00091146-05
NCGC00091146-08
Phenothiazine, purum, >=98.0% (GC)
AC-10429
BP-31210
DA-76809
SY004343
CS-0008338
NS00002986
P0106
SW197745-2
EN300-19084
Phenothiazine, Vetec(TM) reagent grade, 98%
D02601
F90393
AB00572590_12
Phenothiazine, VETRANAL(TM), analytical standard
Q410846
SR-01000721844
SR-01000721844-3
SR-01000721844-4
BRD-K59597909-001-17-6
BRD-K59597909-001-19-2
BRD-K59597909-001-20-0
F0266-2850
Z104472694
Phenothiazine, United States Pharmacopeia (USP) Reference Standard
202-196-5
75788-67-9
InChI=1/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13
Solubility of 10H-phenothiazine
10H-phenothiazine, with the chemical formula C12H9NS, exhibits some interesting solubility characteristics. This compound is known to be:
These properties make 10H-phenothiazine an interesting compound for various applications, particularly in organic synthesis and pharmaceutical chemistry. As emphasized in *solubility studies*, the interaction of solutes with solvents can be complex and highly dependent on environmental factors, which ultimately influence the behavior of 10H-phenothiazine in practical applications.
In summary, while 10H-phenothiazine is largely insoluble in water, its solubility in organic solvents and response to pH changes can offer valuable insights for its utilization in scientific research and industry.