24-1560
吩噻嗪
SAJ first grade
别名:
10H-吩噻嗪
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关于此项目
经验公式（希尔记法）:
C12H9NS
化学文摘社编号:
分子量:
199.27
EC Number:
202-196-5
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
143237
MDL number:
Grade:
SAJ first grade
Bp:
371 °C (lit.)
InChI key
WJFKNYWRSNBZNX-UHFFFAOYSA-N
InChI
1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
SMILES string
N1c2ccccc2Sc3ccccc13
grade
SAJ first grade
availability
available only in Japan
dilution
(for analytical testing)
bp
371 °C (lit.)
mp
182-187 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2 Oral
target_organs
Blood
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Suruchi Mahajan et al.
Advances in colloid and interface science, 199-200, 1-14 (2013-08-13)
Phenothiazine drugs have been the subject of great interest due to their interesting aggregation properties and ability to interact with surfactants, model lipid bilayers, and biomembranes. Since these drugs show enormous pharmacological actions and deposits on the biomembranes, their pharmacological
Photolyase-like repair of psoralen-crosslinked nucleic acids.
Thorsten Stafforst et al.
Angewandte Chemie (International ed. in English), 50(40), 9483-9486 (2011-09-29)
P Halaburda et al.
Talanta, 96, 202-209 (2012-07-24)
A rapid, sensitive and fully automated chemiluminometric method is described for determination of five phenothiazine derivatives, namely, trifluoperazine, fluphenazine, perphenazine, thioridazine and chlorpromazine. The method is based on the chemiluminescence (CL) induced by the oxidation of drugs with Ce(IV) in
Mechanistic basis of phenothiazine-driven inhibition of Tau aggregation.
Elias Akoury et al.
Angewandte Chemie (International ed. in English), 52(12), 3511-3515 (2013-02-13)
Aaron S Hart et al.
ACS applied materials & interfaces, 4(11), 5813-5820 (2012-10-10)
Effect of positioning of the cyanoacrylic acid anchoring group on ring periphery of phenothiazine dye on the performance of dye-sensitized solar cells (DSSCs) is reported. Two types of dyes, one having substitution on the C-3 aromatic ring (Type 1) and
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