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Merck

88580

Sigma-Aldrich

吩噻嗪

purum, ≥98.0% (GC)

别名:

10H-吩噻嗪

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About This Item

经验公式(希尔记法):
C12H9NS
CAS号:
分子量:
199.27
Beilstein:
143237
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

等級

purum

品質等級

化驗

≥98.0% (GC)

形狀

pellets

bp

371 °C (lit.)

mp

182-187 °C (lit.)
183-187 °C

SMILES 字串

N1c2ccccc2Sc3ccccc13

InChI

1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H

InChI 密鑰

WJFKNYWRSNBZNX-UHFFFAOYSA-N

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一般說明

吩噻嗪为刚性、三环结构。已知其可改变多巴胺(3,4-二羟基苯乙胺)。其独特的空穴输运能力、电子释放氮和硫的杂原子以及其非平面结构导致较低的分子聚集,使其可作为电子供体。

應用

吩噻嗪在无金属的有机染料敏化剂、染料 和抗氧化剂中都有应用。

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2 Oral

標靶器官

Blood

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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分析证书(COA)

Lot/Batch Number

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Phenothiazines and butyrophenones are known to alter dopamine (3,4-dihydroxyphenethylamine) metabolism in the brain in a fashion suggesting that they may block dopamine receptors. We observed, using Dreiding molecular models, that dopamine in its solid-state conformation is superimposable upon a portion
Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
Carsten K, et al
Proceedings of the National Academy of Sciences of the USA, 98(17), 9834-9841 (2001)
Asif M, et al
Arabian Journal of Chemistry null
Photodegradation of trimeprazine triggered by self-photogenerated singlet molecular oxygen
Waseem A, et al
Journal of Saudi Chemical Society (2012)
Alina N Sekretaryova et al.
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Wiring glucose oxidase in the membrane with an immobilized mediator is possible due to the diffusion ability of the latter, if the enzyme containing membrane is formed according to the proposed protocol, including exposing proteins to water-organic mixtures with the

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