1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone

Modify Date: 2025-08-24 21:24:10

1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone Structure
1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone structure
Common Name 1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone
CAS Number 89516-38-1 Molecular Weight 416.53500
Density 1.231g/cm3 Boiling Point 679.3ºC at 760 mmHg
Molecular Formula C25H24N2O2S Melting Point N/A
MSDS N/A Flash Point 364.6ºC

 Names

Name 1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone

 Chemical & Physical Properties

Density 1.231g/cm3
Boiling Point 679.3ºC at 760 mmHg
Molecular Formula C25H24N2O2S
Molecular Weight 416.53500
Flash Point 364.6ºC
Exact Mass 416.15600
PSA 74.71000
LogP 5.61510
Index of Refraction 1.643
InChIKey RTWGNRNAFXMGLR-UHFFFAOYSA-N
SMILES CC(=O)c1ccc2c(c1)N(C(=O)CNCCc1ccc(C)cc1)c1ccccc1S2

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
SN5252000
CHEMICAL NAME :
10H-Phenothiazine, 2-acetyl-10-(((2-(4-methylphenyl)ethyl)amino)acetyl)-
CAS REGISTRY NUMBER :
89516-38-1
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C25-H24-N2-O2-S
MOLECULAR WEIGHT :
416.57

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
IJSBDB Indian Journal of Chemistry, Section B: Organic Chemistry, Including Medicinal Chemistry. (Publications & Information Directorate, Council of Scientific and Industrial Research (CSIR), Hillside Rd., New Delhi 110 012, India) V.14B- 1976- Volume(issue)/page/year: 22,952,1983

 Synthetic Route

~59%

1-(2-acetylphenothiazin-10-yl)-2-[2-(4-methylphenyl)ethylamino]ethanone Structure

1-(2-acetylphen...

CAS#:89516-38-1

Literature: Kumar, P.; Nath, C.; Agarwal, Jagdish C.; Bhargava, K. P.; Shanker, K. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1983 , vol. 22, # 9 p. 952 - 954

 Precursor & DownStream

Precursor  2

DownStream  0

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