Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: 4-Thiazolidinone,3-(2-methylphenyl)-2-thioxo-
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Purity: 98.0%
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Contact: Ms Wang

23522-37-4

23522-37-4 structure

23522-37-4 structure

Name: 4-Thiazolidinone,3-(2-methylphenyl)-2-thioxo-
Chemical Name: 3-(2-methylphenyl)-2-sulfanylidene-1,3-thiazolidin-4-one
CAS Number: 23522-37-4
Molecular Formula: C₁₀H₉NOS₂
Molecular Weight: 223.31500
Create Date: 2016-08-18 19:06:10
Modify Date: 2024-01-16 23:49:32

Name	3-(2-methylphenyl)-2-sulfanylidene-1,3-thiazolidin-4-one
Synonyms	2-thioxo-3-o-tolyl-thiazolidin-4-one 2-Thioxo-3-o-tolyl-thiazolidin-4-on

Density	1.39g/cm3
Boiling Point	334.3ºC at 760mmHg
Molecular Formula	C₁₀H₉NOS₂
Molecular Weight	223.31500
Flash Point	156ºC
Exact Mass	223.01300
PSA	77.70000
LogP	2.42470
Vapour Pressure	0.000129mmHg at 25°C
Index of Refraction	1.709

CHEMICAL IDENTIFICATION

RTECS NUMBER :: VI8540000

CHEMICAL NAME :: Rhodanine, 3-(o-tolyl)-

CAS REGISTRY NUMBER :: 23522-37-4

BEILSTEIN REFERENCE NO. :: 0169682

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C10-H9-N-O-S2

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LDLo - Lowest published lethal dose

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: 150 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 19,558,1969

623-51-8 structure

623-51-8

614-69-7 structure

614-69-7

~62%

23522-37-4 structure

23522-37-4

Literature: Karatas; Koni; Dogan Canadian Journal of Chemistry, 1998 , vol. 76, # 3 p. 254 - 259

105-36-2 structure

105-36-2

~%

23522-37-4 structure

23522-37-4

Literature: Hann Journal of the American Chemical Society, 1925 , vol. 47, p. 2000 Chem. Zentralbl., 1924 , vol. 95, # I p. 2110

45892-06-6 structure

45892-06-6

79-11-8 structure

79-11-8

~19%

23522-37-4 structure

23522-37-4

Literature: Aksac, Zihni; Pinar, Esat; Icli, Siddik Organic Magnetic Resonance, 1983 , vol. 21, # 9 p. 548 - 551

68-11-1 structure

68-11-1

614-69-7 structure

614-69-7

~%

23522-37-4 structure

23522-37-4

Literature: Andreasch; Zipser Monatshefte fuer Chemie, 1905 , vol. 26, p. 1193

95-53-4 structure

95-53-4

~%

23522-37-4 structure

23522-37-4

Literature: Aksac, Zihni; Pinar, Esat; Icli, Siddik Organic Magnetic Resonance, 1983 , vol. 21, # 9 p. 548 - 551

6326-83-6 structure

6326-83-6

95-53-4 structure

95-53-4

~%

23522-37-4 structure

23522-37-4

Literature: Holmberg Journal fuer Praktische Chemie (Leipzig), 1910 , vol. <2> 81, p. 456

105-39-5 structure

105-39-5

~%

23522-37-4 structure

23522-37-4

Literature: Andreasch; Zipser Monatshefte fuer Chemie, 1905 , vol. 26, p. 1193

79-07-2 structure

79-07-2

~%

23522-37-4 structure

23522-37-4

Literature: Holmberg; Psilanderhielm Journal fuer Praktische Chemie (Leipzig), 1910 , vol. <2>82, p. 446

Precursor 10
623-51-8 614-69-7 105-36-2 45892-06-6
79-11-8 68-11-1 95-53-4 6326-83-6
105-39-5 79-07-2
DownStream 1
16240-02-1