Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide

Base Information

• Chemical Name: Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide
• CAS No.: 65087-24-3
• Molecular Formula: C29H25 N2 O2 . Br
• Molecular Weight: 513.434
• European Community (EC) Number: 265-405-9
• Mol file: 65087-24-3.mol

Synonyms:3,3'-Diethyl-alpha-naphthoxacarbocyanine bromide;65087-24-3;EINECS 265-405-9;Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propen-1-yl)-, bromide (1:1);Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide;3-Ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)propenyl)naphth(1,2-d)oxazolium bromide

Chemical Property of Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide

Chemical Property:

• PSA: 36.14000
• LogP: 4.18830
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 512.10994
• Heavy Atom Count: 34
• Complexity: 690

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1C2=C(C3=CC=CC=C3C=C2)OC1=CC=CC4=[N+](C5=C(O4)C6=CC=CC=C6C=C5)CC.[Br-]
• Isomeric SMILES: CCN\1C2=C(C3=CC=CC=C3C=C2)O/C1=C/C=C/C4=[N+](C5=C(O4)C6=CC=CC=C6C=C5)CC.[Br-]

Technology Process of Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide

There total 1 articles about Naphth(2,1-d)oxazolium, 3-ethyl-2-(3-(3-ethylnaphth(2,1-d)oxazol-2(3H)-ylidene)-1-propenyl)-, bromide 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:

ethyl ester of p-toluenesulfonic acid (80-40-0) + 2-methyloxazolo<4,5-a>naphthalene (20686-65-1) → 1,3-bis-(3-ethyl-naphth[2,1-d]oxazol-2-yl)-trimethinium ; bromide (65087-24-3)

Guidance literature:

Reaktion ueber mehrere Stufen;

upstream raw materials:

ethyl ester of p-toluenesulfonic acid

2-methyloxazolo<4,5-a>naphthalene

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