Malonaldehyde bis(phenylimine) monohydrochloride

Base Information

• Chemical Name: Malonaldehyde bis(phenylimine) monohydrochloride
• CAS No.: 123071-42-1
• Molecular Formula: C₁₅H₁₄N₂*ClH
• Molecular Weight: 258.75
• DSSTox Substance ID: DTXSID90480711
• NSC Number: 75891
• Mol file: 123071-42-1.mol

Synonyms:123071-42-1;Malonaldehyde bis(phenylimine) monohydrochloride;Malonaldehyde Bis(phenylimine) Hydrochloride;51143-32-9;N,N'-diphenylpropane-1,3-diimine;hydrochloride;Malondialdehyde bis(phenylimine) monohydrochloride;Malondialdehyde dianil hydrochloride;MFCD00054634;N1,n3-diphenylpropane-1,3-diimine xhydrochloride;N1,N3-DIPHENYLPROPANE-1,3-DIIMINE HYDROCHLORIDE;SCHEMBL2960051;SCHEMBL2960053;DTXSID90480711;FLMLOZWXXPLHIE-UHFFFAOYSA-N;malonaldehyde bis(phenylimine) HCl;NSC75891;NSC-75891;AKOS025295386;BP-30146;CS-0207586;malonaldehyde bis(phenylimine)monohydrochloride;E77655;J-004889;Malonaldehyde bis(phenylimine) monohydrochloride, 97%

Chemical Property of Malonaldehyde bis(phenylimine) monohydrochloride

Chemical Property:

• Vapor Pressure: 6.38E-07mmHg at 25°C
• Melting Point: 218 °C (dec.)(lit.)
• Boiling Point: 404 °C at 760 mmHg
• Flash Point: 198.1 °C
• PSA: 24.72000
• LogP: 4.98350
• Storage Temp.: -70°C
• Sensitive.: Hygroscopic
• Water Solubility.: Soluble in water (partly).
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 258.0923762
• Heavy Atom Count: 18
• Complexity: 220

Purity/Quality:

98%Min ^*data from raw suppliers

MalondialdehydeBis(phenylimine)Monohydrochloride ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC=C(C=C1)N=CCC=NC2=CC=CC=C2.Cl
• Uses: Malonaldehyde bis(phenylimine) monohydrochloride is a useful fluorescent cyanine dye.

Technology Process of Malonaldehyde bis(phenylimine) monohydrochloride

There total 1 articles about Malonaldehyde bis(phenylimine) monohydrochloride 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:

malonaldehydebis(dimethylacetal) (102-52-3) + aniline (62-53-3) → malonaldehyde bis(phenylimine) monohydrochloride (51143-32-9,123071-42-1,137692-98-9)

Guidance literature:

Reference yield: 88.0%

1-(ε-carboxypentyl)-2,3,3-trimethyl indolenium-5-sulfonate (749838-12-8) + malonaldehyde bis(phenylimine) monohydrochloride (51143-32-9,123071-42-1,137692-98-9) → 2-[(1E,3E)-4-anilinobuta-1,3-dienyl]-3-methyl-1,3-bis(4-sulfobutyl)-3H-indolium-5-sulfonate (851528-27-3)

Guidance literature:

With acetic anhydride; In acetic acid; at 110 ℃; for 15h;

Reference yield: 88.0%

1-(5-carboxypentyl)-2,3,3-trimethyl-3H-indolium-5-sulfonate (146368-08-3) + malonaldehyde bis(phenylimine) monohydrochloride (51143-32-9,123071-42-1,137692-98-9) → 2-[(1E,3E)-4-anilinobuta-1,3-dienyl]-3-methyl-1,3-bis(4-sulfobutyl)-3H-indolium-5-sulfonate (851528-27-3)

Guidance literature:

With acetic anhydride; acetic acid; at 110 ℃; for 15h;

upstream raw materials:

malonaldehydebis(dimethylacetal)

aniline

Downstream raw materials:

1,5-bis-(3-ethyl-6-styryl-benzothiazol-2-yl)-pentamethinium; bromide

1,5-bis-[5-(2-cyano-vinyl)-3-ethyl-benzothiazol-2-yl]-pentamethinium; toluene-4-sulfonate

1,5-bis-(8-ethyl-thiazolo[4',5':3,4]benzo[1,2-c][1,2,5]thiadiazol-7-yl)-pentamethinium; toluene-4-sulfonate

1,5-bis-(8-ethyl-thiazolo[4',5':3,4]benzo[1,2-c][1,2,5]selenadiazol-7-yl)-pentamethinium; toluene-4-sulfonate

Refernces