Basic information Safety Supplier Related

4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid

Basic information Safety Supplier Related

4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid Basic information

Product Name:
4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid
Synonyms:
  • 4-METHYL-2-N-PROPYL-1H-BENZIMIDAZOLE-6-CARBOXYLIC ACID
  • 4-METHYL-2-PROPYL-1H-BENZIMIDAZOLE-6-CARBOXYLIC ACID
  • 4-METHYL-2-PROPYL-6-CARBOXYL BENZIMIDAZOLE
  • 2-N-PROPYL-4-METHYL-6-CARBOXY-BENZIMIDAZOLE
  • 2-N-PROPYL-4-METHYLBENZIMIDAZOLE-6-CARBOXYLIC ACID
  • 2-PROPYL-4-METHYL-6-CARBOXYL BENZIMIDAZOLE
  • Telmisartan Intermediate 3
  • 2-N-Propyl-4-Meth
CAS:
152628-03-0
MF:
C12H14N2O2
MW:
218.25
EINECS:
424-450-6
Product Categories:
  • Heterocycles
  • Imidazoles
  • Aromatics
  • INTERMEDIATESOF
  • Imidazol&Benzimidazole
Mol File:
152628-03-0.mol
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4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid Chemical Properties

Melting point:
300 °C
Boiling point:
491.8±25.0 °C(Predicted)
Density 
1.259±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO, Methanol
pka
3.19±0.30(Predicted)
form 
Powder
color 
Pale Yellow to Tan
InChIKey
XWAJTVCEILFDGU-UHFFFAOYSA-N
CAS DataBase Reference
152628-03-0(CAS DataBase Reference)
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Safety Information

HS Code 
29332900
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4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid Usage And Synthesis

Chemical Properties

Light Yellow to Tan Powder

Uses

4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid is a useful synthetic intermediate,a useful compound in organic synthesis.

Synthesis

152628-01-8

152628-03-0

Example 4: Methyl 3-methyl-4-butyrylamino-5-nitrobenzoate (II) (10 g, 0.036 mol) was suspended in 60 ml of water and heated to 70-80 °C. A suspension of sodium dithionite (21.75 g, 0.124 mol) in 60 ml of water was added slowly and heated to 90-100 °C. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 10-11 and the temperature was maintained with continued stirring until TLC detection showed complete disappearance of methyl 3-methyl-4-butyrylamino-5-nitrobenzoate. Subsequently, the pH of the reaction mixture was adjusted to 6-6.5. The resulting solid was filtered and dried at 45-50 °C to afford 2-n-propyl-4-methyl-6-carboxybenzimidazole (7.5 g, yield: 96.4%).

References

[1] Patent: WO2012/28925, 2012, A2. Location in patent: Page/Page column 18
[2] Journal of Heterocyclic Chemistry, 2003, vol. 40, # 6, p. 1107 - 1112
[3] Journal of Medicinal Chemistry, 1993, vol. 36, # 25, p. 4040 - 4051
[4] Patent: WO2012/28925, 2012, A2
[5] Organic Process Research and Development, 2007, vol. 11, # 1, p. 81 - 85

4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid Preparation Products And Raw materials

Raw materials

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