2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride

Base Information

• Chemical Name: 2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride
• CAS No.: 93089-86-2
• Molecular Formula: C₉H₈N₂O₂*ClH
• Molecular Weight: 212.636
• European Community (EC) Number: 805-701-2
• Mol file: 93089-86-2.mol

Synonyms:2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride;93089-86-2;2-methyl-3H-benzimidazole-5-carboxylic acid;hydrochloride;2-Methyl-1H-benzimidazole-5-carboxylic acid hydrochloride;SCHEMBL7331906;2-Methyl-1H-benzoimidazole-5-carboxylic acid hydrochloride;MBTOZVMYBGBPOH-UHFFFAOYSA-N;GEO-02476;AKOS015996301;CS-0232744;EN300-128450;2-methylbenzimidazole-5-carboxylic acid hydrochloride;Z1622825549;2-methyl-1 h-benzoimidazole-5-carboxylic acid hydrochloride;2-Methyl-1H-benzo[d]imidazole-5-carboxylicacidhydrochloride;2-methyl-1h-benzoimidazole-5-carboxylic acid, hydrochloride;2-Methyl-1H-benzo[d]imidazole-5-carboxylic acid hydrochloride

Chemical Property of 2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 212.0352552
• Heavy Atom Count: 14
• Complexity: 220

Purity/Quality:

99% ^*data from raw suppliers

2-methyl-1H-1,3-benzodiazole-5-carboxylicAcidhydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=NC2=C(N1)C=C(C=C2)C(=O)O.Cl

Technology Process of 2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride

There total 1 articles about 2-methyl-1H-1,3-benzodiazole-5-carboxylic acid hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3,4-diaminobenzoic acid (619-05-6) → 2-methyl-1(3)H-benzimidazole-5-carboxylic acid ; hydrochloride (93089-86-2)

Guidance literature:

With hydrogenchloride; acetic acid;

Reference yield:

2-methyl-1(3)H-benzimidazole-5-carboxylic acid ; hydrochloride (93089-86-2) → methyl 2-methylbenzimidazole-5-carboxylate hydrochloride (106429-51-0)

Guidance literature:

With hydrogenchloride; sodium hydroxide; In methanol; water;

upstream raw materials:

3,4-diaminobenzoic acid

Downstream raw materials:

methyl 2-methylbenzimidazole-5-carboxylate hydrochloride