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Product Name: 2-[(2-chloroethyl-nitroso-carbamoyl)amino]acetamide
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65267-04-1

65267-04-1 structure

65267-04-1 structure

Name: 2-[(2-chloroethyl-nitroso-carbamoyl)amino]acetamide
Chemical Name: 2-[[2-chloroethyl(nitroso)carbamoyl]amino]acetamide
CAS Number: 65267-04-1
Molecular Formula: C₅H₉ClN₄O₃
Molecular Weight: 208.60300
Create Date: 2017-07-05 21:11:59
Modify Date: 2025-08-24 22:55:03

Name	2-[[2-chloroethyl(nitroso)carbamoyl]amino]acetamide
Synonyms	1-(Carbamoylmethyl)-3-(2-chloroethyl)-3-nitrosourea Urea,1-(carbamoylmethyl)-3-(2-chloroethyl)-3-nitroso N-<N'-(2-chloroethyl)-N'-nitrosocarbamoyl>glycinamide 2-(3-(2-chloroethyl))-3-nitrosoureido acetamide n2-[(2-chloroethyl)(nitroso)carbamoyl]glycinamide

Density	1.58g/cm3
Molecular Formula	C₅H₉ClN₄O₃
Molecular Weight	208.60300
Exact Mass	208.03600
PSA	104.86000
LogP	0.49470
Index of Refraction	1.597

CHEMICAL IDENTIFICATION

RTECS NUMBER :: YS4552830

CHEMICAL NAME :: Urea, 1-(carbamoylmethyl)-3-(2-chloroethyl)-3-nitroso-

CAS REGISTRY NUMBER :: 65267-04-1

LAST UPDATED :: 199612

DATA ITEMS CITED :: 2

MOLECULAR FORMULA :: C5-H9-Cl-N4-O3

MOLECULAR WEIGHT :: 208.63

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 :: 21230 ug/kg

TOXIC EFFECTS :: Tumorigenic - active as anti-cancer agent

REFERENCE :: JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 25,829,1982

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 22400 ug/kg

TOXIC EFFECTS :: Tumorigenic - active as anti-cancer agent

REFERENCE :: JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 25,829,1982

60784-40-9 structure

60784-40-9

1668-10-6 structure

1668-10-6

~40%

65267-04-1 structure

65267-04-1

Literature: Eisenbrand; Gerhard Patent: US4150146 A1, 1979 ;

55661-43-3 structure

55661-43-3

598-41-4 structure

598-41-4

~73%

65267-04-1 structure

65267-04-1

Literature: Suami; Kato; Takino; Hisamatsu Journal of Medicinal Chemistry, 1982 , vol. 25, # 7 p. 829 - 832

80354-49-0 structure

80354-49-0

598-41-4 structure

598-41-4

~51%

65267-04-1 structure

65267-04-1

Literature: Sosnovsky; Gnewuch Journal of Pharmaceutical Sciences, 1994 , vol. 83, # 7 p. 989 - 998

Precursor 4
1668-10-6 55661-43-3 598-41-4 80354-49-0
DownStream 0

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