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Merck
CN

24-1560

Phenothiazine

SAJ first grade

Synonym(s):

10H-Phenothiazine

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About This Item

Empirical Formula (Hill Notation):
C12H9NS
CAS Number:
92-84-2
Molecular Weight:
199.27
EC Number:
202-196-5
UNSPSC Code:
12352005
PubChem Substance ID:
329752589
Beilstein/REAXYS Number:
143237
MDL number:
MFCD00005015
Grade:
SAJ first grade
Bp:
371 °C (lit.)

Key Documents

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Product Name

Phenothiazine, SAJ first grade

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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Warning

Hazard Classifications

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

target_organs

Blood

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
U2891
U2179
U4432
U2685
A9243

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Caiwen Ou et al.
Chemical communications (Cambridge, England), 49(18), 1853-1855 (2013-01-31)
We report a 'super-gelator' of a short peptide capped with phenothiazine acetic acid.
Gabriela B Rodrigues et al.
Journal of photochemistry and photobiology. B, Biology, 116, 89-94 (2012-09-18)
Photodynamic antimicrobial chemotherapy (PACT) is a promising alternative to conventional chemotherapy that can be used to treat localized mycosis. The development of PACT depends on identifying effective and selective PS for the different pathogenic species. The in vitro susceptibilities of
M L Buck et al.
DICP : the annals of pharmacotherapy, 25(3), 244-247 (1991-03-01)
A two-month-old white girl presented to our facility with increasing lethargy and new onset apnea and bradycardia following a week of upper respiratory tract infection symptoms. The patient had been receiving a cough syrup containing promethazine hydrochloride during the previous
Maike J Ohlow et al.
Drug discovery today, 16(3-4), 119-131 (2011-01-18)
Rooted in the early days of organic dye chemistry, the phenothiazine structure and its derivatives have since held a prominent place in pharmacology and biomedicine. Initially used for histochemical stains of plasmodia by Paul Ehrlich, anthelmintic and antibiotic properties of
Dalila Belei et al.
Bioorganic & medicinal chemistry letters, 22(14), 4517-4522 (2012-06-29)
The biological screening of the chemical library of our Organic Chemistry Department, carried out on an automated fluorescence-based FTase assay, allowed us to discover that a phenothiazine derivative (1d) was an inhibitor of farnesyltransferase. Three new series of human farnesyltransferase
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