Interesting facts
Exploring Methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate
Methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate is a fascinating chemical compound with distinct properties and potential applications. Here are some intriguing aspects of this compound:
- Biological Relevance: Compounds like this one often belong to a class of chemicals that demonstrate significant biological activity. The benzimidazole structure is known for its role in pharmacology, particularly as a scaffold for drug design. Researchers are particularly interested in how modifications, such as the inclusion of a propylsulfanyl group, can enhance therapeutic efficacy.
- Insecticidal Properties: Many carbamate derivatives exhibit insecticidal properties. The structural characteristics of methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate suggest potential use as an agricultural pesticide, contributing to pest management strategies in sustainable agriculture.
- Synthetic Versatility: The synthetic pathways leading to this compound can involve a variety of reactions, showcasing the versatility of organic synthesis techniques. Understanding these methods is crucial for chemists looking to create novel compounds with unique properties.
- Research Applications: Ongoing studies are examining the interactions of this compound with various biological systems, aiming to uncover mechanisms of action that are both fascinating and applicable in the fields of medicine and agriculture.
In summary, methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate stands as a promising compound in the nexus of chemistry and biology. As scientists continue to explore its diverse applications, this compound could play a pivotal role in the development of new treatments and sustainable agricultural practices.
Synonyms
albendazole
54965-21-8
Albenza
Eskazole
Zentel
Valbazen
Albendazol
Proftril
Albendazolum
Andazol
SK&F 62979
Methyl 5-(propylthio)-2-benzimidazolecarbamate
SKF 62979
5-(Propylthio)-2-carbomethoxyaminobenzimidazole
SK&F-62979
Albendazol [INN-Spanish]
Albendazolum [INN-Latin]
methyl N-[6-(propylsulfanyl)-1H-1,3-benzodiazol-2-yl]carbamate
methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate
MFCD00083232
NSC 220008
HSDB 7444
(5-(Propylthio)-1H-benzimidazol-2-yl)carbamic acid methyl ester
EINECS 259-414-7
O-Methyl N-(5-(propylthio)-2-benzimidazolyl)carbamate
NSC-220008
Albendazole(Albenza)
DTXSID0022563
UNII-F4216019LN
CHEBI:16664
Carbamic acid, [5-(propylthio)-1H-benzimidazol-2-yl]-, methyl ester
CARBAMIC ACID, (5-(PROPYLTHIO)-1H-BENZIMIDAZOL-2-YL)-, METHYL ESTER
((Propylthio)-5 1H-benzimidazolyl-2) carbamate de methyle
Bilutac
F4216019LN
CHEMBL1483
DTXCID202563
methyl [6-(propylsulfanyl)-1H-benzimidazol-2-yl]carbamate
Zental
methyl N-[5-(propylsulfanyl)-1H-1,3-benzodiazol-2-yl]carbamate
NSC220008
Albendazole [USAN:USP:INN:BAN:JAN]
methyl [5-(propylsulfanyl)-1H-benzimidazol-2-yl]carbamate
NCGC00016876-01
CAS-54965-21-8
Albendazol (INN-Spanish)
Albendazolum (INN-Latin)
ALBENDAZOLE (MART.)
ALBENDAZOLE [MART.]
ALBENDAZOLE (USP-RS)
ALBENDAZOLE [USP-RS]
methyl [5-(propylthio)-1H-benzimidazol-2-yl]carbamate
methyl 5-(propylthio)-1H-benzo[d]imidazol-2-ylcarbamate
Methyl [5-(Propylthio)benzimidazol-2-yl]carbamate
SKF-62979
ALBENDAZOLE (EP MONOGRAPH)
ALBENDAZOLE [EP MONOGRAPH]
ALBENDAZOLE (USP MONOGRAPH)
ALBENDAZOLE [USP MONOGRAPH]
methyl (NZ)-N-(5-propylsulfanyl-1,3-dihydrobenzimidazol-2-ylidene)carbamate
Albendazole (USAN:USP:INN:BAN:JAN)
Albenza (TN)
Albendazole (JAN/USP/INN)
Zenteltrade mark
[5-(Propylthio)benzimidazol-2-yl]carbamic Acid Methyl Ester
Albenzatrade mark
Andazoltrade mark
Eskazoletrade mark
Albendazole,(S)
((Propylthio)-5 1H-benzimidazolyl-2) carbamate de methyle [French]
Prestwick_675
Albendazole200 mg
Albendazole (Albenza)
Albendazole (Standard)
Spectrum_001532
CPD000036735
Albendazole 100 microg/mL in Acetonitrile
ALBENDAZOLE [MI]
(5-Propylsulfanyl-1H-benzoimidazol-2-yl)-carbamic acid methyl ester
methyl 5-propylthio-2-benzimidazolecarbamate
Prestwick0_000247
Prestwick1_000247
Prestwick2_000247
Prestwick3_000247
Spectrum4_000201
Spectrum5_001567
ALBENDAZOLE [INN]
ALBENDAZOLE [JAN]
ChemDivAM_000003
ChemDiv1_000190
ALBENDAZOLE [HSDB]
ALBENDAZOLE [USAN]
ALBENDAZOLE [VANDF]
Oprea1_429292
Oprea1_585016
Oprea1_640007
SCHEMBL44682
ALBENDAZOLE [WHO-DD]
ALBENDAZOLE [WHO-IP]
BSPBio_000034
BSPBio_002548
KBioGR_000801
KBioSS_002012
MLS000069722
ALBENDAZOLUM [WHO-IP]
BIDD:GT0615
DivK1c_000704
SPECTRUM1503903
methoxy-N-(5-propylthiobenzimidazol-2-yl)carboxamide
SPBio_002253
BPBio1_000038
ALBENDAZOLE [GREEN BOOK]
HMS502D06
HMS587I14
HXHWSAZORRCQMX-UHFFFAOYSA-
HY-B0223R
KBio1_000704
KBio2_002012
KBio2_004580
KBio2_007148
ALBENDAZOLE [ORANGE BOOK]
P02CA03
NINDS_000704
GLXC-20304
HMS1568B16
HMS1922K04
HMS2090G19
HMS2093K13
HMS2095B16
HMS2231O03
HMS3259B05
HMS3369C03
HMS3651C15
HMS3712B16
Pharmakon1600-01503903
[5-(Propythio)-1H-benzimidazol-2-yl]carbamic acid methyl ester
BCP12108
HY-B0223
Tox21_110659
Tox21_302300
AC-015
BBL005883
BDBM50241293
CCG-39620
MFCD01220143
N-[6-(propylthio)-1H-benzimidazol-2-yl]carbamic acid methyl ester
NSC758644
s1640
STK387550
STL046130
AKOS000540882
AKOS005431684
AKOS005699352
Tox21_110659_1
CCG-220247
DB00518
FA30267
KS-5159
NC00615
NSC-758644
IDI1_000704
methyl [(2Z)-5-(propylsulfanyl)-1,3-dihydro-2H-benzimidazol-2-ylidene]carbamate
NCGC00016876-02
NCGC00016876-03
NCGC00016876-04
NCGC00016876-05
NCGC00016876-06
NCGC00016876-07
NCGC00016876-08
NCGC00016876-09
NCGC00016876-10
NCGC00016876-12
NCGC00022896-03
NCGC00022896-04
NCGC00022896-05
NCGC00022896-06
NCGC00022896-07
NCGC00022896-08
NCGC00255250-01
Albendazole 50 microg/mL in Acetonitrile
Albendazole, analytical standard, >=98%
SMR000036735
SY052519
SBI-0051849.P002
DB-052669
A1943
AB00052377
NS00009208
SW196830-3
5-(propylthio)-2-carbomethoxyaminobenzimazole
EN300-49850
methyl 5-propylthio-2-benzimidazole carbamate
VU0239747-6
BIM-0051849.0001
C01779
D00134
H10782
AB00052377-13
AB00052377-14
AB00052377_15
AB00052377_16
A830429
Q411629
SR-01000000171
SR-05000001875
SR-01000000171-2
SR-05000001875-1
BRD-K79131256-001-04-7
BRD-K79131256-001-08-8
BRD-K79131256-001-17-9
BRD-K79131256-001-18-7
METHYL 5-(PROPYLTHIO)BENZIMIDAZOL-2-YLCARBAMATE
methyl 6-(propylthio)-1H-benzo[d]imidazol-2-ylcarbamate
Z594284186
2-[(Methoxycarbonyl)amino]-5-propylthio-1H-benzimidazole
Albendazole, European Pharmacopoeia (EP) Reference Standard
methyl (5-(propylthio)-1H-benzo[d]imidazol-2-yl)carbamate
Methyl (6-(propylthio)-1H-benzo[d]imidazol-2-yl)carbamate
Methyl 5-(propylsulfanyl)-1H-benzimidazol-2-ylcarbamate #
methyl N-(5-propylsulfanyl-1H-benzimidazol-2-yl)carbamate
Albendazole, United States Pharmacopeia (USP) Reference Standard
METHYL N-(5-(PROPYLTHIO)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
Albendazole, Pharmaceutical Secondary Standard; Certified Reference Material
Carbamic acid, N-[5-(propylthio)-1H-benzimidazol-2-yl]-,?methyl ester
259-414-7
InChI=1/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
Solubility of Methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate
Methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate, with the chemical formula C12H15N3O2S, presents unique solubility characteristics that can impact its practical applications in various fields. The solubility of this compound can be influenced by several factors:
In practical applications, it is essential to consider these factors when attempting to dissolve methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate. As a general rule, “like dissolves like”—meaning that nonpolar solvents would be more effective in solubilizing nonpolar portions of the molecule, while polar solvents would better accommodate its polar regions. Therefore, for effective utilization, one must assess the most suitable solvent environment in which to work with this compound.