Interesting facts
Interesting Facts About Methyl N-(1H-benzimidazol-2-yl)carbamate
Methyl N-(1H-benzimidazol-2-yl)carbamate is a fascinating compound that captures the interest of chemists and biochemists alike. Here are some notable points about this intriguing molecule:
- Biological Significance: This compound is derived from benzimidazole, a well-known structure in medicinal chemistry, which has shown promise in various pharmacological applications, including anti-cancer and anti-parasitic properties.
- Mechanism of Action: The core benzimidazole ring imparts distinctive reactivity that can interact with biological targets, potentially modifying vital enzymatic processes.
- Research Insights: Studies have indicated that methyl N-(1H-benzimidazol-2-yl)carbamate can play a role in developing new agrochemicals, enhancing crop resistance against pests and diseases.
- Synthetic Routes: Chemists have developed various synthetic methodologies to produce this compound, showcasing its versatility and importance in both academic research and industry.
- Pharmacological Potential: The compound is currently explored for its potential use in drug discovery, particularly in the design of novel therapeutic agents targeting specific diseases.
As highlighted by researchers, "The exploration of benzimidazole derivatives remains a key focus in innovative drug development." This reflects the continuous quest in the chemical sciences to unlock new pathways for health and agricultural advancements.
The integration of methyl N-(1H-benzimidazol-2-yl)carbamate into various fields—from pharmaceuticals to sustainability initiatives—demonstrates its multifaceted importance in today’s scientific landscape.
Synonyms
Carbendazim
10605-21-7
Carbendazole
Mecarzole
Bavistin
Thicoper
Carbendazime
Bavistan
Carbendazol
Derosal
Funaben
Medamine
Carbendazym
Equitdazin
Garbenda
Kemdazin
Supercarb
Agrizim
Battal
Bengard
Bitosen
Custos
Delsene
Karben
Kolfugo
Stempor
BMK (fungicide)
Methyl 2-benzimidazolecarbamate
Myco
Methyl benzimidazol-2-ylcarbamate
Bavistin 3460
carbendazine
Falicarben
Fungisol
Pillarstin
Triticol
Stein
Spin
Bercema-Bitosen
Kolfugo Extra
Carbamic acid, 1H-benzimidazol-2-yl-, methyl ester
methyl N-(1H-benzimidazol-2-yl)carbamate
Preventol BCM
Antibac MF
Carben VL
Funaben 3
BCM (fungicide)
Jkatein
Funaben 50
Benzimidazolecarbamic
IPO Y
2-MBC
METHYL 1H-BENZIMIDAZOL-2-YLCARBAMATE
Methyl benzimidazolylcarbamate
Preparation G 665
A 118 (pesticide)
carbendazin
carbendazyme
mekarzole
2-(Methoxycarbamoyl)benzimidazole
Lignasan
2-(Carbomethoxyamino)benzimidazole
Kolfugo 25 FW
Methyl 1H-benzimidazole-2-carbamate
1H-Benzimidazole-2-carbamic acid, methyl ester
2-(Methoxycarbonylamino)-benzimidazole
BAS 67054F
2-(Methoxycarbonylamino)benzimidazole
2-Benzimidazolecarbamic acid, methyl ester
Bavistine
Derroprene
Jkstein
Zhiweiling
Methyl N-2-benzimidazolecarbamate
1H-Benzimidazol-2-ylcarbamic acid methyl ester
BAS-3460
CTR 6669
Bavistin FL
EK 578
HOE 17411
CCRIS 1553
Spin (pesticide)
Benzimidazole-2-carbamic acid, methyl ester
Carbendazim [BSI:ISO]
methyl-2-benzimidazole carbamate
2-(Methoxy-carbonylamino)-benzimidazol
G 665
Olgin (fungicide)
Bavistin 25SD
Bavistin 50SD
HSDB 6581
Delsene 10
Derosal 60PM
Kolfugo 25FW
IPO-1250
U 32104
BA 67054F
methyl 2-benzimidazil carbamate
Methyl 2-benzimidazolylcarbamate
methylbenzimidazole-2-ylcarbamate
BAS 3460F
Benzimidazole carbamate de methyle
benzimidazolecarbamate methyl ester
BAS 3460 F
IPO 1250
methoxybenzimidazole-2-carbamic acid
BMK
EINECS 234-232-0
methyl-N-(2-benzimidazolyl)carbamate
BAS-67054
FB-642
EPA Pesticide Chemical Code 115001
EPA Pesticide Chemical Code 128872
NSC 109874
NSC-109874
UNII-H75J14AA89
1H-Benzimidazol-2-ylcarbamic acid, methyl ester
2-[(Methoxycarbonyl)amino]benzimidazole
2-Methyl benzimidazolecarbamate
CHEBI:3392
2-benzimidazolecarbamic acid methyl ester
DTXSID4024729
U-32.104
BAS-67054F
H75J14AA89
2-(Methoxycarboxamido)benzimidazole
A 118
BAS 3460
CTR-6669
EK-578
DTXCID004729
1H-Benzimidazol-2-yl-carbamic acid, methyl ester
HOE-17411
NSC109874
A118
METHYL N-1H-BENZIMIDAZOL-2-YLCARBAMATE
ALBENDAZOLE IMPURITY E (EP IMPURITY)
ALBENDAZOLE IMPURITY E [EP IMPURITY]
2-((METHOXYCARBONYL)AMINO)BENZIMIDAZOLE
FB642
carb
Carbenzadime
Cekudazim
MCAB
Methyl benzimidazolycarbamate
methyl-2-benzimidazolecarbamate
methoxycarbonylaminobenzimidazole
N-2-(benzimidazolyl) carbamate
methyl benzimidazole-2-ylcarbamate
methyl benzimidazol-2-yl carbamate
Methyl bendimidazole-2-yl-carbamate
methyl benzimidazole-2-yl carbamate
Methyl-alpha-benzimidazole Carbamate
BAS 67054
FB 642
Methyl 1H-benzemedazol-2-ylcarbamate
N-2-(BENZIMIDAZOLYL)CARBAMATE
methyl-1h-benzimidazol-2-yl carbamate
methyl (1h-benzimidazol-2-yl)carbamate
USEPA/OPP Pesticide Code: 128872
2-Benzimidazolecarcamic Acid Methyl Ester
234-232-0
bcm
bmc
methyl 1H-benzo[d]imidazol-2-ylcarbamate
Mercarzole
BMK (VAN)
Methyl benzimidazolecarbamate
Fungoxan
Protek
Sarfun
Subeej
Karben flo Stefes
Karben Stefes Flo
Carbendazim D3
105268-95-9
Methyl 1H-benzimidazolylcarbamate
Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester
CHEMBL70971
MLS002701961
Methyl 1H-benzimidazol-2-ylcarbamate (9CI)
methyl N-(1H-1,3-benzodiazol-2-yl)carbamate
2-(Methoxy-carbonylamino)-benzimidazol [German]
Carbamic acid, 1H-benzimidazolyl-, methyl ester
N-benzimidazol-2-ylmethoxycarboxamide
37953-07-4
2-Bezimidazolecarbamic acid methyl ester
39413-19-9
MBC (VAN)
Carbendazim 100 microg/mL in Methanol
Carbendazime [ISO-French]
Carbamic acid, N-1H-benzimidazol-2-yl-, methyl ester;Methyl 1H-benzo[d]imidazol-2-ylcarbamate
Carbendazim (MBC)
Carbendazim [ISO]
CAS-10605-21-7
2-(Methoxy-carbonylamino)-benzimidazol (GERMAN)
RCRA waste no. U372
Carbate
Benzimidazole carbamate de methyle [French]
Benomyl metabolite
Carbendazol, JMAF
Tripart defensor FL
Carbendazim, 97%
Turfclear (Salt/Mix)
Carbendazim (Standard)
BMC?
CARBENDAZIM [MI]
ChemDivAM_000201
ChemDiv1_000052
CARBENDAZIM [HSDB]
SCHEMBL21051
CARBENDAZIM [WHO-DD]
N-1H-Benzimidazol-2-yl-carbamic Acid Methyl Ester
BIDD:ER0282
SCHEMBL2706729
SCHEMBL4977926
Carbendazim, analytical standard
2-carbomethoxyamino-benzimidazole
methyl benzimidazole-2-carbamate
HMS587C08
methyl 2-benzimidazolyl-carbamate
HMS5081H18
KID PEST PROJECT (CARBENDAZIM) (SEE ALSO CARBENDAZIM)
Tox21_202295
Tox21_300478
2-(carbomethoxy-amino)-benzimidazole
BDBM50116313
HY-13582R
Methyl 1H-2-benzimidazolecarbaminate
Methyl N-benzimidazol-2-yl-carbamate
MFCD00055390
SBB057110
Carbendazim 50 microg/mL in Methanol
AKOS002384358
CCG-101273
CS-8030
DB13009
IC19689
KS-5360
2-(Methoxy-carbonylamino)-benzimidazole
NCGC00090706-01
NCGC00090706-02
NCGC00090706-03
NCGC00090706-04
NCGC00254328-01
NCGC00259844-01
AC-10590
BP-21318
HY-13582
NCI60_000240
SMR000304463
ST020591
DB-040676
Methyl 1H-benzimidazol-2-ylcarbamate, 9CI
FENBENDAZOLE IMPURITY A [EP IMPURITY]
NS00010265
S3676
Carbendazim, PESTANAL(R), analytical standard
E78626
EN300-180487
A801368
AF-962/00515023
Q418607
SR-01000390861
(1H-Benzoimidazol-2-yl)-carbamic acid methyl ester
SR-01000390861-1
BRD-K12906202-001-06-2
Carbendazim, certified reference material, TraceCERT(R)
F0266-0908
Z752774256
Fenbendazole impurity A, European Pharmacopoeia (EP) Reference Standard
N-1H-Benzimidazol-2-yl-carbamic acid methyl ester;2-Benzimidazolecarbamic acid methyl ester;Albendazole impurity E;Carbendazole
Solubility of Methyl N-(1H-benzimidazol-2-yl)carbamate
Methyl N-(1H-benzimidazol-2-yl)carbamate, often referred to for its unique structural features, displays interesting solubility characteristics in various solvents.
In summary, while methyl N-(1H-benzimidazol-2-yl)carbamate may not be significantly soluble in water, its compatibility with a range of polar and apolar organic solvents highlights its versatility in chemical applications. The ability to dissolve in various media is crucial for its effectiveness in formulations such as pharmaceuticals and agrochemicals.