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ABERCHROME 670

Base Information Edit
  • Chemical Name:ABERCHROME 670
  • CAS No.:94856-25-4
  • Molecular Formula:C22H24O4
  • Molecular Weight:352.43
  • Hs Code.:
  • Mol file:94856-25-4.mol
ABERCHROME 670

Synonyms:Aberchrome670

Suppliers and Price of ABERCHROME 670
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Aberchrome 670
  • 25mg
  • $ 75.00
  • TRC
  • Aberchrome 670
  • 2.5mg
  • $ 45.00
  • TCI Chemical
  • Aberchrome 670 >98.0%(HPLC)
  • 1g
  • $ 292.00
  • Biosynth Carbosynth
  • Aberchrome 670
  • 2 g
  • $ 90.00
  • Biosynth Carbosynth
  • Aberchrome 670
  • 1 g
  • $ 50.00
  • Biosynth Carbosynth
  • Aberchrome 670
  • 5 g
  • $ 187.50
  • Biosynth Carbosynth
  • Aberchrome 670
  • 10 g
  • $ 300.00
  • American Custom Chemicals Corporation
  • 2- (2- ADAMANTYLIDENE) - 3- [1- (2, 5- DIMETHYL- 3- FURANYL) ETHYLIDENE] - SUCCINANHYDRIDE 95.00%
  • 5MG
  • $ 497.20
  • AK Scientific
  • Aberchrome 670
  • 2g
  • $ 171.00
  • AK Scientific
  • Aberchrome 670
  • 1g
  • $ 117.00
Total 11 raw suppliers
Chemical Property of ABERCHROME 670 Edit
Chemical Property:
  • Melting Point:175-185°C 
  • PSA:56.51000 
  • LogP:4.50600 
Purity/Quality:

98%,99%, *data from raw suppliers

Aberchrome 670 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses ABERCHROME 670 is a photochromic compound.
Technology Process of ABERCHROME 670

There total 11 articles about ABERCHROME 670 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 420 g / NaH / toluene; paraffin / 45 - 50 °C
2: dicyclohexylcarbodiimide / CH2Cl2 / 3 h
3: 1) NaH, 2) 10percent ethanolic KOH / 1) toluene, mineral oil, 2) reflux, 4 h
4: AcCl / CH2Cl2 / 3 h
With potassium hydroxide; sodium hydride; acetyl chloride; dicyclohexyl-carbodiimide; In dichloromethane; toluene; paraffin;
Guidance literature:
Multi-step reaction with 3 steps
1: dicyclohexylcarbodiimide / CH2Cl2 / 3 h
2: 1) NaH, 2) 10percent ethanolic KOH / 1) toluene, mineral oil, 2) reflux, 4 h
3: AcCl / CH2Cl2 / 3 h
With potassium hydroxide; sodium hydride; acetyl chloride; dicyclohexyl-carbodiimide; In dichloromethane;
Guidance literature:
Multi-step reaction with 2 steps
1: 1) NaH, 2) 10percent ethanolic KOH / 1) toluene, mineral oil, 2) reflux, 4 h
2: AcCl / CH2Cl2 / 3 h
With potassium hydroxide; sodium hydride; acetyl chloride; In dichloromethane;
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