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Home > Encyclopedia > 2-MERCAPTO-5-METHOXYBENZIMIDAZOLE

2-MERCAPTO-5-METHOXYBENZIMIDAZOLE

2-MERCAPTO-5-METHOXYBENZIMIDAZOLE structure

2-MERCAPTO-5-METHOXYBENZIMIDAZOLE 

structure
  • CAS No:

    37052-78-1

  • Formula:

    C8H8N2OS

  • Chemical Name:

    2-MERCAPTO-5-METHOXYBENZIMIDAZOLE

  • Synonyms:

    5-Methoxye-2-mercaplobenzinidazole;TIMTEC-BB SBB000219;5-METHOXY-1H-BENZO[D]IMIDAZOLE-2-THIOL;5-Methoxybenzimidazole-2-thiol;5-METHOXY-2-THIOBENZIMIDAZOLE;5-METHOXY-2-MERCAPTOBENZIMIDAZOLE;5-METHOXY-2-BENZIMIDAZOLETHIOL;2-MERCAPTO-5-METHOXY-1H-BENZIMIDAZOLE

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

2-Mercapto-5-methoxybenzimidazole is used in the preparation of COX-2 inhibitors. It is also employed in the preparation of compounds such as 5-methoxy-2[[(4-methoxy-3, 5-dimethyl-2-pyridinyl) methyl] sulfonyl]-1H-benzimidazole, 5-methoxy-2[[(4-methoxy-3, 5-dimethylpyridin-2-yl-1-oxide) methyl] sulfonyl]-1H-benzimidazole as well as tris[μ-1,2-bis(diphenylphosphino)ethane]-1:2κ2P:P′;1:3κ2P:P′;2:3κ2P:P′-di-μ-bromido-1:2κ4Br:Br-bromido-3κBr-tricopper(I) acetone hemisolvate. Furthermore, it acts as a hetercocyclic building block and serves as an intermediate of drug omeprazole1. Finally, it acts as an intermediate for manufacture of the anti-ulcer drug Omeprazole.


off-white to light yellowish-brown powder


Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

2-MERCAPTO-5-METHOXYBENZIMIDAZOLE Basic Attributes

180.23

180.23

3605123

253-326-2

143562LXX0

DTXSID20190558

Off-white to light yellow-brown

29332900

Characteristics

1.2425 (rough estimate)

261-263 °C(lit.)

309.4±44.0 °C(Predicted)

1.5690 (estimate)

insoluble

0.001Pa at 25℃

Not classified

10.13±0.30(Predicted)

2-8°C

Safety Information

IRRITANT

3

Xi,Xn

26-36

36/37/38-37-22

|Danger|H302 (47.83%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P261, P264, P270, P271, P272, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P307+P311, P312, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 115 companies from 16 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-MERCAPTO-5-METHOXYBENZIMIDAZOLE Use and Manufacturing

Reagent used in the synthesis of COX-2 inhibitors


2-Mercapto-5-methoxybenzimidazole is used in the preparation of COX-2 inhibitors. It is also employed in the preparation of compounds such as 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfonyl]-1H-benzimidazole and 5-methoxy-2-[[(4-methoxy-3,5-dimethylpyridin-2-yl-1-oxide)methyl]sulfonyl]-1H-benzimidazole. Further, it acts as a hetercocyclic building block and serves as an intermediate of drug omeprazole.


5-Methoxy-2-benzimidazolethiol may be used in the preparation of compounds present as contaminants in omeprazole, such as 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfonyl]-1H-benzimidazole and 5-methoxy-2-[[(4-methoxy-3,5-dimethylpyridin-2-yl-1-oxide)methyl]sulfonyl]-1H-benzimidazole. It may be used in the synthesis of tris[μ-1,2-bis(diphenylphosphino)ethane]-1:2κ2P:P′;1:3κ2P:P′;2:3κ2P:P′-di-μ-bromido-1:2κ4Br:Br-bromido-3κBr-tricopper(I) acetone hemisolvate.

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