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N-(PHENYLTHIO)PHTHALIMIDE

CAS No.
14204-27-4
Chemical Name:
N-(PHENYLTHIO)PHTHALIMIDE
Synonyms
N-(PHENYLTHIO)PHTHALIMIDE;N-(Phenylthio)phthalimide>N-(Phenylthio)phthalimide;2-(Phenylthio)isoindoline-1,3-dione;2-(Phenylthio)-1,3-isoindolinedione;2-(Phenylthio)-1H-isoindol-1,3(2H)-dione;2-(Phenylthio)-1H-isoindole-1,3(2H)-dione;1H-Isoindole-1,3(2H)-dione, 2-(phenylthio)-
CBNumber:
CB1240906
Molecular Formula:
C14H9NO2S
Molecular Weight:
255.29
MDL Number:
MFCD00192396
MOL File:
14204-27-4.mol
Last updated:2023-04-23 13:52:06

N-(PHENYLTHIO)PHTHALIMIDE Properties

Melting point 160-163 °C(lit.)
Boiling point 432.2±28.0 °C(Predicted)
Density 1.42±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO: soluble25mg/mL, clear, yellow
pka -3.05±0.20(Predicted)
form powder to crystal
color White to Light yellow
CAS DataBase Reference 14204-27-4

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  24/25
WGK Germany  3
HS Code  29309090

N-(PHENYLTHIO)PHTHALIMIDE price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical P1254 N-(Phenylthio)phthalimide >98.0%(GC)(N) 14204-27-4 5g $94 2024-03-01 Buy
TCI Chemical P1254 N-(Phenylthio)phthalimide >98.0%(GC)(N) 14204-27-4 25g $372 2024-03-01 Buy
TRC P399325 N-(Phenylthio)phthalimide 14204-27-4 50mg $45 2021-12-16 Buy
American Custom Chemicals Corporation CHM0156787 N-(PHENYLTHIO)PHTHALIMIDE 95.00% 14204-27-4 5G $880.94 2021-12-16 Buy
American Custom Chemicals Corporation CHM0156787 N-(PHENYLTHIO)PHTHALIMIDE 95.00% 14204-27-4 25G $1407.4 2021-12-16 Buy
Product number Packaging Price Buy
P1254 5g $94 Buy
P1254 25g $372 Buy
P399325 50mg $45 Buy
CHM0156787 5G $880.94 Buy
CHM0156787 25G $1407.4 Buy

N-(PHENYLTHIO)PHTHALIMIDE Chemical Properties,Uses,Production

Preparation

(a) Preparation of benzenesulfenyl chloride. To a stirred solution of 55 gm (0.5 mole) of benzene thiol in 300 ml of η -pentane at 0°C is added chlorine gas until an assay (GC) of the resulting red-orange solution shows quantitative conversion to the sulfenyl chloride. The reaction usually re­quires about 39 gm (0.6 mole) of chlorine.
(b) Reaction of benzenesulfenyl chloride with phthalimide. To a stirred solution of 73.5 gm (0.5 mole) of phthalimide in 200 ml of dimethylforma-mide is first added 60 gm (0.6 mole) of triethylamine. Then the sulfenyl chloride solution from (a) is slowly added dropwise. The reaction mixture is stirred for \ hr, poured into 2 liters of cold water, filtered, and dried to afford 121 gm (95%), m.p. 160-161°C (recrystallized from ethanol).
Complex imides such as camphorimide and 9,10-dihydroanthracene-9,10-endo-a,/3-succinimide have been alkylated in methylene dichloride with alkyl halides, using tetrabutylammonium bromide as a phase-transfer catalyst and aqueous potassium hydroxide as a base.
Preparation of N-(Phenylthio)phthalimide

N-(PHENYLTHIO)PHTHALIMIDE Preparation Products And Raw materials

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TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24539 81
N-(Phenylthio)phthalimide 2-(Phenylthio)-1,3-isoindolinedione 2-(Phenylthio)isoindoline-1,3-dione N-(PHENYLTHIO)PHTHALIMIDE N-(Phenylthio)phthalimide> 1H-Isoindole-1,3(2H)-dione, 2-(phenylthio)- 2-(Phenylthio)-1H-isoindole-1,3(2H)-dione 2-(Phenylthio)-1H-isoindol-1,3(2H)-dione 14204-27-4 Building Blocks Others Organic Building Blocks Sulfur Compounds Sulfur Compounds (for Synthesis) N-Substituted Phthalimides N-Substituted Maleimides, Succinimides & Phthalimides N-Substituted Phthalimides Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry Organic Building Blocks Others Sulfur Compounds Building Blocks Chemical Synthesis Organic Building Blocks Sulfur Compounds N-Substituted Maleimides, Succinimides & Phthalimides