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13245-90-4

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13245-90-4 Usage

Physical state

Solid

Color

Bright yellow

Solubility

Sparingly soluble in water, soluble in organic solvents

Uses

a. Reagent in organic synthesis
b. Exhibits antimicrobial properties
c. Exhibits anticancer properties

Applications

a. Production of pharmaceuticals
b. Production of agrochemicals
c. Production of other fine chemicals

Structural features

a. Aromatic ring system
b. Double bond structure

Safety precautions

a. Potential skin and eye irritant
b. Potentially harmful if ingested or inhaled
c. Handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 13245-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13245-90:
(7*1)+(6*3)+(5*2)+(4*4)+(3*5)+(2*9)+(1*0)=84
84 % 10 = 4
So 13245-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H16/c1-3-10-18(11-4-1)22(19-12-5-2-6-13-19)21-16-15-17-9-7-8-14-20(17)21/h1-16H

13245-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzhydrylideneindene

1.2 Other means of identification

Product number -
Other names 6,6-diphenyl-1,2-benzofulvene

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:13245-90-4 SDS

13245-90-4Relevant articles and documents

-

Alt, Helmut G.,Jung, Michael,Kehr, Gerald

, p. 153 - 181 (2007/10/03)

Twenty-three new ansa metallocene complexes of the type (C13H8-CR2-C9H6-nR′ n)ZrCl2 (38-64) (n=0, 1; R=Me, Ph, butenyl; R′=alkyl, alkenyl) and the corresponding ligand precursors have been synthesized and characterized. The bonding situation of the π-ligands to the metal of C1-bridged complexes in solution was determined by NMR-spectroscopy. All complexes were tested for catalytic ethylene polymerization after activation with methyl aluminoxane (MAO). The substituents R in the bridge and the substituents R′ in the 3-position of the indenylidene moiety have a strong influence on the activity of the catalysts and the molecular weight of the formed polymers. The ω-alkenyl substituents R and R′ allow self-immobilization of the catalysts during the polymerization.

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