Cambendazol structure
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Common Name | Cambendazol | ||
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CAS Number | 26097-80-3 | Molecular Weight | 302.352 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | N/A | |
Molecular Formula | C14H14N4O2S | Melting Point | 212-214℃ (ethyl acetate hexane ) | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS08 |
Signal Word | Warning |
Use of CambendazolCambendazole is one of the most effective agents for the therapy of human strongyloidiasis and [1]. |
Name | propan-2-yl N-[2-(1,3-thiazol-4-yl)-3H-benzimidazol-5-yl]carbamate |
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Synonym | More Synonyms |
Description | Cambendazole is one of the most effective agents for the therapy of human strongyloidiasis and [1]. |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Melting Point | 212-214℃ (ethyl acetate hexane ) |
Molecular Formula | C14H14N4O2S |
Molecular Weight | 302.352 |
Exact Mass | 302.083740 |
PSA | 108.14000 |
LogP | 2.90 |
Index of Refraction | 1.694 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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~% Cambendazol CAS#:26097-80-3 |
Literature: Merck and Co., Inc. Patent: US3956488 A1, 1976 ; |
~% Cambendazol CAS#:26097-80-3 |
Literature: Rajappa, S.; Sreenivasan, R. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1980 , vol. 19, # 7 p. 539 - 541 |
~% Cambendazol CAS#:26097-80-3 |
Literature: Rajappa, S.; Sreenivasan, R. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1980 , vol. 19, # 7 p. 539 - 541 |
~% Cambendazol CAS#:26097-80-3 |
Literature: Rajappa, S.; Sreenivasan, R. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1980 , vol. 19, # 7 p. 539 - 541 |
The Hymenolepis diminuta-golden hamster (Mesocricetus auratus) model for the evaluation of gastrointestinal anticestode activity.
J. Parasitol. 90(4) , 898-9, (2004) A novel laboratory anticestode assay was developed using Hymenolepis diminuta in the hamster. The commercial anticestode compounds, praziquantel, bunamidine, and niclosamide were active against patent... |
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Structural requirements for the induction of cytochromes P450 by benzimidazole anthelmintic derivatives in cultured rabbit hepatocytes.
Biochem. Biophys. Res. Commun. 220(3) , 789-94, (1996) The effect of sulfur-containing benzimidazoles (thiabendazole, 5-hydroxy-thiabendazole, cambendazole) and sulfur-free derivatives (benzimidazole, carbendazim and 5-hydroxycarbendazim) on cytochrome P4... |
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Controlled tests of activity of several antiparasitic compounds against natural infections of Haemonchus contortus and other helminths in lambs from a flock established in 1962.
Am. J. Vet. Res. 54(3) , 406-10, (1993) Antiparasitic activity of several compounds was evaluated over a long period (about 25 years) in the same flock of sheep. Haemonchus contortus was of special interest, including its relation to drug r... |
Cambenzole |
Carbamic acid, N-[2-(4-thiazolyl)-1H-benzimidazol-6-yl]-, 1-methylethyl ester |
Novazole |
Isopropyl [2-(1,3-thiazol-4-yl)-1H-benzimidazol-5-yl]carbamate |
Equiben |
Camvet |
(2-thiazol-4-yl-1(3)H-benzoimidazol-5-yl)-carbamic acid isopropyl ester |
CBDZ |
propan-2-yl [2-(1,3-thiazol-4-yl)-1H-benzimidazol-5-yl]carbamate |
cambendazole |
Carbamic acid, (2-(4-thiazolyl)-1H-benzimidazol-5-yl)-, 1-methylethyl ester |
Isopropyl 2-(4-thiazolyl)-5-benzimidazolecarbamate |
NOE [French] |
Noviben |
Bonlam |
[2-(4-thiazolyl)-1H-benzimidazol-5-yl]carbamic acid 1-methylethyl ester |
5-isopropoxycarbonylamino-2-(4'-thiazolyl)-benzimidazole |
Camdan |
Cambendazol |