Welcome to LookChem.com Sign In|Join Free

CAS

  • or

85223-10-5

Post Buying Request

85223-10-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,2'-[[(4-chlorophenyl)methyl](phenylmethyl)amino]-6'-(dibutylamino)-

    Cas No: 85223-10-5

  • USD $ 1.0-1.0 / Metric Ton

  • 1 Metric Ton

  • 100 Metric Ton/Day

  • Bluecrystal chem-union
  • Contact Supplier
  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,2'-[[(4-chlorophenyl)methyl](phenylmethyl)amino]-6'-(dibutylamino)-

    Cas No: 85223-10-5

  • No Data

  • No Data

  • No Data

  • Antimex Chemical Limied
  • Contact Supplier
  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,2'-[[(4-chlorophenyl)methyl](phenylmethyl)amino]-6'-(dibutylamino)-

    Cas No: 85223-10-5

  • No Data

  • No Data

  • No Data

  • kingstonchem
  • Contact Supplier

85223-10-5 Usage

Commonly known as

BAPTA-xanthene

Properties

spiroxanthene-based compound

Potential applications

Fluorescent calcium indicator in biological research
Potential use in photodynamic therapy for cancer treatment
Investigated as a photosensitizer in the development of organic light-emitting diodes (OLED)
Fluorescent probe for other metal ions

Unique chemical structure

Contains benzylamino and dibutylamino groups
Contains a spiroxanthene moiety
Versatile compound with potential uses in various fields of research and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 85223-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85223-10:
(7*8)+(6*5)+(5*2)+(4*2)+(3*3)+(2*1)+(1*0)=115
115 % 10 = 5
So 85223-10-5 is a valid CAS Registry Number.

85223-10-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-[benzyl-[(4-chlorophenyl)methyl]amino]-6'-(dibutylamino)spiro[2-benzofuran-3,9'-xanthene]-1-one

1.2 Other means of identification

Product number -
Other names EINECS 286-363-8

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85223-10-5 SDS

85223-10-5Downstream Products

85223-10-5Relevant articles and documents

HIGHLY EFFICIENT METHOD FOR PRODUCING SATURATED HOMOETHER FROM UNSATURATED CARBONYL COMPOUND

-

Paragraph 0049; 0051-0052, (2020/07/16)

PROBLEM TO BE SOLVED: To provide a method for efficiently producing a saturated homoether from an unsaturated carbonyl compound. SOLUTION: The method for producing an unsaturated homoether uses an unsaturated carbonyl compound and hydrogen as a raw material, uses a catalyst comprising a metal supported on an acidic catalyst carrier and performs at least once a pressure reduction operation so that a differential pressure from a reaction pressure is 0.01 MPa or more. In the method, the metal of the catalyst is, for example, palladium and the carrier of the catalyst is alumina, silica, silica-alumina or the like. The unsaturated carbonyl compound serving as a raw material is 2-butenal, 2-ethyl-2-hexenal, 2-ethyl-2-butenal, 2-hexenal or the like and the produced saturated homoether is dibutyl ether, bis(2-ethylhexyl)ether, bis(2-ethylbutyl)ether, dihexyl ether or the like. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Copper promoter effect on acid-base and redox sites of Fe/Al2O3 catalysts and their role in ethanol-acetone mixture conversion

Pinheiro, Antonio Narcisio,Dos Santos, Regina Claudia Rodrigues,Ferreira Dos Santos, Sarah Brenda,Da Silva Júnior, Moacir José,Pinheiro Braga, Tiago,Freire, Valder Nogueira,Valentini, Antoninho

, p. 443 - 458 (2018/02/07)

Active species of copper and iron oxide (Cu-Fe) catalysts supported on alumina were prepared by combining Pechini and wet impregnation methods. The effect of combined acid-base and redox sites of Cu and Fe species on gas-phase ethanol-acetone mixture conversion was investigated. The catalysts were characterized by chemical analyses, XRD, H2-TPR, M?ssbauer spectroscopy, N2 physisorption, CO2-TPD, SEM-EDS, TG/DTA and pyridine adsorption isotherms. N2 adsorption/desorption isotherms and SEM-EDS analysis showed that the addition of copper caused an increase of BET surface area and Cu and Fe oxide dispersion. H2-TPR characterization showed that interactions between Cu and Fe oxides shift the reducibility of Fe3+ species to lower temperature improving the redox properties of the catalyst. The partial reduction of the Cu and Fe oxide species was found to be efficient in inhibiting the side decomposition reactions, improving the catalytic efficiency towards dehydrogenation and hydrogen transfer processes. It was found that acid-base pairs play an important role in the formation of dehydrogenation, dehydration and condensation products from ethanol, while redox sites are decisive for hydrogen transfer reactions with reduction of acetone to isopropanol. H2-TPR and M?ssbauer spectroscopy results for the spent catalysts revealed that the highest catalytic performance of the Cu-FeAl catalysts may be attributed to the good dispersion of the Cu oxide and the site generated by the partial reduction which produces Cu+/Cu0 and Fe2+ active species. A reaction pathway with the participation of the acid-base and redox sites in the formation of products by consecutive dehydrogenation-condensation or dehydrogenation-hydrogenation reactions has been proposed.

Preparation method of key intermediate 2-ethyl butyraldehyde of 2-ethyl butyric acid

-

Paragraph 0011-0012, (2017/07/19)

The invention provides a preparation method of a key intermediate, 2-ethyl butyraldehyde, of 2-ethyl butyric acid, wherein the preparation method includes the steps of: adding an ethyl magnesium halide Grignard reagent to a protected alpha-halogenated aldehyde (I) solution, and performing a stirring reaction for 1-10 h at a certain temperature; performing post-treatment and de-protecting the product to obtain the 2-ethyl butyraldehyde. A route in the process in represented as follows. The method has short route and high usage ratio, is low in cost and easy to industrialize, and avoids defects in conventional methods.

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 85223-10-5