C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-)

Base Information

• Chemical Name: C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-)
• CAS No.: 1032678-07-1
• Molecular Formula: C₃₂H₃₉N₂O₂*Cl
• Molecular Weight: 519.127

Synonyms:C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-)

Chemical Property of C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-)

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

Cy5acid 96% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Description: Cy5 acid is a dye containing a non-activated carboxylic acid. This dye has limited water solubility, but can be dissolved in mixtures of water with organic phase (DMF, DMSO, alcohols) to obtain useful concentrations of the material in solution. This molecule can be considered non-reactive dye for the use in control samples, and for instrument calibration.

Technology Process of C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-)

There total 10 articles about C₃₂H₃₉N₂O₂⁽¹⁺⁾*Cl^(1-) 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: 74.0%

1,3,3-trimethyl-2-((1E,3E)-4-(N-phenylacetamido)buta-1,3-dien-1-yl)-3H-indolium chloride (1127303-67-6) + 1-(5-carboxypentyl)-2,3,3-trimethyl-3H-indol-1-ium iodide (865611-47-8) → C32H39N2O2(1+)*Cl(1-) (1032678-07-1)

Guidance literature:

With pyridine; at 23 - 50 ℃; for 1.5h; Inert atmosphere;

DOI:10.1021/ja206339s

Reference yield: 67.0%

1-(5-carboxypentyl)-2,3,3-trimethylindoleninium bromide + malonaldehyde bis(phenylimine) monohydrochloride (51143-32-9,123071-42-1,137692-98-9) + 1,2,3,3-tetramethyl-3H-indolium iodide (5418-63-3) → 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-(5-carboxypentyl)-3H-indolium chloride (1032678-07-1)

Guidance literature:

1-(5-carboxypentyl)-2,3,3-trimethylindoleninium bromide; malonaldehyde bis(phenylimine) monohydrochloride; With acetic anhydride; at 120 ℃; for 0.5h;

1,2,3,3-tetramethyl-3H-indolium iodide; With pyridine; acetic anhydride; at 20 ℃; for 12h;

DOI:10.1002/ejoc.200701190

Reference yield: 48.0%

1-(5-carboxypentyl)-2,3,3-trimethyl-3H-indol-1-ium iodide (865611-47-8) + malonaldehyde bis(phenylimine) monohydrochloride (51143-32-9,123071-42-1,137692-98-9) + 1,2,3,3-tetramethyl-3H-indolium iodide (5418-63-3) → 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-(5-carboxypentyl)-3H-indolium chloride (1032678-07-1)

Guidance literature:

1-(5-carboxypentyl)-2,3,3-trimethyl-3H-indol-1-ium iodide; malonaldehyde bis(phenylimine) monohydrochloride; With acetic anhydride; at 130 ℃; for 0.5h;

1,2,3,3-tetramethyl-3H-indolium iodide; With pyridine; at 20 ℃;

DOI:10.1002/chem.201700563

upstream raw materials:

malonaldehyde bis(phenylimine) monohydrochloride

1,2,3,3-tetramethyl-3H-indolium iodide

1-(5-carboxypentyl)-2,3,3-trimethyl-3H-indol-1-ium iodide

2,3,3-trimethylindoleniune

Downstream raw materials:

2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride

2-[5-(1,3,3-trimethyl-2,3-dihydroindol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(trans-4-hydroxycyclohexylaminocarbonyl)pentyl]-3H-indolium hexafluorophosphate

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