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Lobendazole

HCID 22752
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Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
6306-71-4
Standard SMILES
CCOC(=O)Nc1nc2ccccc2[nH]1
InChIKey
OKOVSTKGUBOSTB-UHFFFAOYSA-N
Molecular formula
C10H11N3O2
Average molar mass
205.21 g/mol
Monoisotopic mass
205.0851266

Overview

N-(1H-benzimidazol-2-yl)carbamic acid ethyl ester is a member of benzimidazoles and a carbamate ester.

Names & identifiers

Preferred name
Lobendazole
IUPAC
ethyl N-(1H-benzimidazol-2-yl)carbamate
English name
Lobendazole
Molecular formula
C10H11N3O2
Molecular weight
205.21

Names & synonyms

Lobendazole6306-71-4NSC-42044LobendazolEthyl 2-benzimidazolecarbamateLobendazolumSK&F 24529SK&F-24529CMF6Z78SWLDTXSID70212390NSC42044RefChem:924867
Show more names
G-756F 24529SKF-24529AIDS-089126SK and F-245292-Benzimidazolecarbamic acid, ethyl ester
DTXCID70134881ethyl N-(1H-benzimidazol-2-yl)carbamateethyl (1H-benzo[d]imidazol-2-yl)carbamateethyl 1H-benzo[d]imidazol-2-ylcarbamateEthyl 1H-benzimidazol-2-ylcarbamate2-CarboethoxyaminobenzimidazoleEthyl 2-benzimidazolylcarbamateN-(2'-Benzimidazolyl)-urethane

Database identifiers

CAS
6306-71-4
PubChem CID
22752
DTXSID
DTXSID70212390
ChEMBL
CHEMBL2105088
ChEBI
CHEBI:92287
UNII
CMF6Z78SWL
Nikkaji
J9.596F

Properties

Computed structural properties

XLogP
1.9
Topological polar surface area
67 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
3
Rotatable bonds
3
Heavy atoms
15
Formal charge
0
Complexity
235

Experimental & physicochemical properties

Collision Cross Section · 2 items

141.7 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

139.92 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

Physicochemical properties

Melting point
320 °C · 320 °C (decomp)
Density
1.358 · 1.358
pka
10.78 · 10.78±0.10(Predicted)
FDA UNII
6 Z78SWL · CMF6Z78SWL

Chemistry & industry

Applications

UsesAnthelmintic (veterinary).

UsesEthyl (1H-Benzo[d]imidazol-2-yl)carbamate is used in method of making 1-(Acyloxy)-alkyl Carbamate prodrugs of amine containing drugs.

Suppliers15 total

上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]
杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
韶关市启程生物科技有限公司18122215013 · [email protected]
上海皓鸿生物医药科技有限公司400-8210725 4008210725 · [email protected]
北京福源坊科技有限公司010-57903446 15869909019 · [email protected]
Alfa Chemistry+1-5166625404 · [email protected]
艾吉析科技(上海)有限公司17717235263 17717235263 · [email protected]
上海阿拉丁生化科技股份有限公司6206333 13167063860 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海睿升化工科技有限公司15026594951 · [email protected]
上海康恩博医药科技有限公司(科小研试剂)400-1388-521 17510465506 · [email protected]
砌块化学科技(上海)有限公司021-20432219 13918097649 · [email protected]
重庆卡兰医药有限公司[email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
合肥钼凯医药科技有限公司18001872185; 18001872185 · [email protected]

Additional notes

DefinitionChEBI: N-(1H-benzimidazol-2-yl)carbamic acid ethyl ester is a member of benzimidazoles and a carbamate ester.

Related reactions

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Compound notes

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