1-Ethyl-2-(2-((1-ethylnaphtho(1,2-d)thiazol-2(1H)-ylidene)methyl)-1-buten-1-yl)naphtho(1,2-d)thiazolium bromide

Base Information

• Chemical Name: 1-Ethyl-2-(2-((1-ethylnaphtho(1,2-d)thiazol-2(1H)-ylidene)methyl)-1-buten-1-yl)naphtho(1,2-d)thiazolium bromide
• CAS No.: 3028-94-2
• Molecular Formula: C31H29 N2 S2 . Br
• Molecular Weight: 573.621
• European Community (EC) Number: 221-195-0
• Mol file: 3028-94-2.mol

Synonyms:4,5,4',5'-dibenzo-3,3'-9-triethylthiacarbocyanine bromide1-ethyl-2-(3-(1-ethylnaphtho(1,2d)thiazolin-2- ylidene)-2-ethylpropenyl)naphtho(1,2D)thiazolium;ethyl-stains-all;triethyl-carbocyanin DBTC

Chemical Property of 1-Ethyl-2-(2-((1-ethylnaphtho(1,2-d)thiazol-2(1H)-ylidene)methyl)-1-buten-1-yl)naphtho(1,2-d)thiazolium bromide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 65.29000
• Density: g/cm³
• LogP: 5.11040
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 572.09555
• Heavy Atom Count: 36
• Complexity: 745

Purity/Quality:

99% ^*data from raw suppliers

ETHYL STAINS-ALL 95.00% ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(=CC1=[N+](C2=C(S1)C=CC3=CC=CC=C32)CC)C=C4N(C5=C(S4)C=CC6=CC=CC=C65)CC.[Br-]
• Isomeric SMILES: CC/C(=C/C1=[N+](C2=C(S1)C=CC3=CC=CC=C32)CC)/C=C\4/N(C5=C(S4)C=CC6=CC=CC=C65)CC.[Br-]

Technology Process of 1-Ethyl-2-(2-((1-ethylnaphtho(1,2-d)thiazol-2(1H)-ylidene)methyl)-1-buten-1-yl)naphtho(1,2-d)thiazolium bromide

There total 1 articles about 1-Ethyl-2-(2-((1-ethylnaphtho(1,2-d)thiazol-2(1H)-ylidene)methyl)-1-buten-1-yl)naphtho(1,2-d)thiazolium 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:

→ 2-ethyl-1,3-bis-(1-ethyl-naphtho[1,2-d]thiazol-2-yl)-trimethinium ; bromide (3028-94-2)

Guidance literature:

/BRN= 3858759/;