2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide

Modify Date: 2024-04-08 21:02:30

2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide Structure
2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide structure
Common Name 2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide
CAS Number 62292-40-4 Molecular Weight 322.76700
Density 1.43g/cm3 Boiling Point 585.2ºC at 760 mmHg
Molecular Formula C14H11ClN2O3S Melting Point N/A
MSDS N/A Flash Point 307.7ºC

 Names

Name 2-Chloro-N-{4-[(4-nitrophenyl)-thio]phenyl}acetamide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.43g/cm3
Boiling Point 585.2ºC at 760 mmHg
Molecular Formula C14H11ClN2O3S
Molecular Weight 322.76700
Flash Point 307.7ºC
Exact Mass 322.01800
PSA 100.22000
LogP 4.51950
Index of Refraction 1.665

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AB5820500
CHEMICAL NAME :
Acetamide, 2-chloro-N-(4-((4-nitrophenyl)thio)phenyl)-
CAS REGISTRY NUMBER :
62292-40-4
LAST UPDATED :
199612
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C14-H11-Cl-N2-O3-S
MOLECULAR WEIGHT :
322.78
WISWESSER LINE NOTATION :
WNR DSR DMV1G

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 :
2 gm/kg
TOXIC EFFECTS :
Brain and Coverings - recordings from specific areas of CNS Behavioral - somnolence (general depressed activity) Biochemical - Metabolism (Intermediary) - effect on inflammation or mediation of inflammation
REFERENCE :
EJMCA5 European Journal of Medicinal Chemistry--Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 13,93,1978
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2 gm/kg
TOXIC EFFECTS :
Brain and Coverings - recordings from specific areas of CNS Behavioral - somnolence (general depressed activity) Biochemical - Metabolism (Intermediary) - effect on inflammation or mediation of inflammation
REFERENCE :
EJMCA5 European Journal of Medicinal Chemistry--Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 13,93,1978

 Safety Information

HS Code 2930909090

 Synthetic Route

~%

2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide Structure

2-Chloro-N-[4-[...

CAS#:62292-40-4

Literature: Abbady, M. A.; Ali, M. M.; Kandeel, M. M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1981 , vol. 20, # 1 p. 53 - 57

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide
4'-Nitro-4-chlorocetamido-diphenylsulfide
2-chloro-4'-(p-nitrophenylthio)acetanilide
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