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5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole

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5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole Basic information

Product Name:
5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole
Synonyms:
  • 5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole
  • 5-[4'-METHYL (1,1'-BIPHENYL)-2-YL]-1-TRIPHENYLMETHYL-TETRAZOLE
  • 5-[2-(4-methylphenyl)phenyl]-1-trityltetrazole
  • N-(Triphenylmethyl)-5-(4'-Methylbiphenyl-2-Yl-)Tetrazole (Ttmb)
  • Olmesartan TTMB impurity
  • 1-[2-(diphenylmethyl)phenyl]-5-[2-(4-methylphenyl)phenyl]tetrazole
  • Losartan Impurity 9
  • n-(triphenylmethyl)-5-(4'-methylbiphenyl-2-yl-)terazole
CAS:
124750-53-4
MF:
C33H26N4
MW:
478.59
Product Categories:
  • Biphenyl & Diphenyl ether
  • API intermediates
  • Hypertension
Mol File:
124750-53-4.mol
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5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole Chemical Properties

Melting point:
166-169 °C(Solv: ethyl acetate (141-78-6); dichloromethane (75-09-2))
Boiling point:
681.6±65.0 °C(Predicted)
Density 
1.13±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly)
form 
Solid
pka
0.30±0.10(Predicted)
color 
Off-White
CAS DataBase Reference
124750-53-4(CAS DataBase Reference)
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5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole Usage And Synthesis

Chemical Properties

Off-white Solid

Uses

An intermediate in the preparation of labelled Candesartan.

Uses

5-?(4''-?Methyl-?[1,?1''-?biphenyl]?-?2-?yl)?-?1-?trityl-?1H-?tetrazole is a reactant in the synthesis of anti-microbial agents.

Synthesis

5-(4'-Methylbiphenyl-2-yl)-1-trityl-1H-tetrazole is prepared by the reaction of trityl chloride and 2-(tetrazol-5-yl)-4'-methyl-1,1'-biphenyl. The specific synthesis steps are as follows:
Dissolve compound 2 (200 g) with stirring at 40°C 700mL of acetone, Aqueous sodium hydroxide solution (40.67 g sodium hydroxide dissolved in 160 mL water) is added, Continue stirring for 1h, A solution of triphenylchloromethane in acetone (270.8 g of triphenylmethyl chloride dissolved in 800 mL of acetone) was initially added dropwise. The solid was added dropwise and gradually evolved into a white turbid liquid. The reaction was monitored by TLC until it was completely filtered off and washed with water to give a solid as intermediate 3. The solid was blow dried at 50°C to give white intermediate 3 (385 g), yield: 95.2%, HPLC: 99.44%.

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