2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-

Base Information

• Chemical Name: 2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-
• CAS No.: 91-92-9
• Deprecated CAS: 496861-62-2
• Molecular Formula: C36H28N2O6
• Molecular Weight: 584.628
• European Community (EC) Number: 202-108-5
• NSC Number: 50679,37224
• DSSTox Substance ID: DTXSID0059033
• Mol file: 91-92-9.mol

Synonyms:NAPHTHOL AS-BR;91-92-9;Azotol DA;Azoic Coupling Component 3;Naphtanilide BR;Sanatol BR;Amarthol AS-BR;Naphtol AS-BR;Hiltonaphthol AS-BR;Acco Naphthol AS-BR;Amanil Naphthol AS-BR;C.I. Azoic Coupling Component 3;C.I. 37575;2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-;Naphthol AS-BR C.I. 37575;EINECS 202-108-5;NSC 37224;2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy(1,1'-biphenyl)-4,4'-diyl)bis(3-hydroxy-;4', 3,3''-dihydroxy-;C36H28N2O6;3,3'-Dihydroxy-N,N'-(3,3'-dimethoxybiphenyl-4,4'-diyl)di-2-naphthamide;2-Naphthalenecarboxamide,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-;n,n'-(3,3'-dimethoxybiphenyl-4,4'-diyl)bis(3-hydroxynaphthalene-2-carboxamide);3-hydroxy-N-[4-[4-[(3-hydroxynaphthalene-2-carbonyl)amino]-3-methoxyphenyl]-2-methoxyphenyl]naphthalene-2-carboxamide;DTXSID0059033;SCHEMBL11094894;CCG-2510;NSC37224;NSC50679;NSC-37224;NSC-50679;AKOS001482915;C36-H28-N2-O6;MS-30460;HY-121932;CS-0083691;4',4'''-Bi-2-naphth-o-anisidide, 3,3''-dihydroxy-;3,3'-dihydroxy-N,N'-(3,3'-dimethoxybiphenyl-4,4'-diyl)di-2-naphthamid;N,N'-(3,3'-dimethoxybiphenyl-4,4'-diyl)bis(3-hydroxy-2-naphthamide);2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'- biphenyl]-4,4'-diyl)bis[3-hydroxy-

Chemical Property of 2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-

Chemical Property:

• Boiling Point: 701.2°Cat760mmHg
• Flash Point: 377.9°C
• PSA: 117.12000
• Density: 1.373g/cm³
• LogP: 7.73900
• XLogP3: 8.1
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 584.19473662
• Heavy Atom Count: 44
• Complexity: 902

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=CC(=C1)C2=CC(=C(C=C2)NC(=O)C3=CC4=CC=CC=C4C=C3O)OC)NC(=O)C5=CC6=CC=CC=C6C=C5O

Technology Process of 2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy-

There total 2 articles about 2-Naphthalenecarboxamide, N,N'-(3,3'-dimethoxy[1,1'-biphenyl]-4,4'-diyl)bis[3-hydroxy- 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:

3,3'-dimethoxy-(1,1'-biphenyl)-4,4'-diamine (119-90-4) + 3-Hydroxy-2-naphthoic acid (92-70-6) → 4,4'-bis-(3-hydroxy-naphthalene-2-carbonylamino)-3,3'-dimethoxy-biphenyl (91-92-9)

Guidance literature:

With toluene; phosphorus trichloride;

Reference yield:

→ 4,4'-bis-(3-hydroxy-naphthalene-2-carbonylamino)-3,3'-dimethoxy-biphenyl (91-92-9)

Guidance literature:

3,3'-Dimethoxy-benzidin, 3-Hydroxy-naphthoyl-(2)-chlorid, Xylol;

upstream raw materials:

3,3'-dimethoxy-(1,1'-biphenyl)-4,4'-diamine

3-Hydroxy-2-naphthoic acid

Refernces

Contribution of phosphates and adenine to the potency of adenophostins at the IP₃ receptor: Synthesis of all possible bisphosphates of adenophostin A

10.1021/jm201571p

The study investigated the role of different phosphate groups and adenosine motifs in adenophostin A (AdA), a potent agonist of the D-inositol 1,4,5-triphosphate receptor (IP3R). The researchers synthesized all three possible diphosphate analogs of AdA and glucose 3,4-bisphosphate (7). They found that 2-dephospho-AdA (6), which mimics Ins(4,5)P2, was only 4-fold less potent than IP3, while 7 was 400-fold less potent. Even 3″-dephospho-AdA (5), which lacks one vicinal diphosphate group, has measurable activity. This study concludes that the adenosine motif has a direct role in promoting adenylate cyclase potency that is independent of the 2′-phosphate group and that the vicinal diphosphate motif is not essential for IP3R activity. The results suggest that it may be possible to design potent agonists using only two of the three phosphates, and a model for possible interaction with adenine-R504 supports the activity of 5 and 6.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 91-92-9 Naphthol AS-BR C.I. 37575

Send

Send

Metric Ton KG G Pound L ML

Send

Send