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14404-25-2

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14404-25-2 Usage

Chemical Properties

deep red crystals

Check Digit Verification of cas no

The CAS Registry Mumber 14404-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14404-25:
(7*1)+(6*4)+(5*4)+(4*0)+(3*4)+(2*2)+(1*5)=72
72 % 10 = 2
So 14404-25-2 is a valid CAS Registry Number.
InChI:InChI=1/4CHO.2Cl.2Rh/c4*1-2;;;;/h4*2H;;;;/rC4H4Cl2O4Rh2/c7-1-11(2-8)5-12(3-9,4-10)6-11/h7-10H

14404-25-2SDS

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 dis-chloro-bis[dicar

1.2 Other means of identification

Product number -
Other names Rhodium chlorodicarbonyl dimer

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:14404-25-2 SDS

14404-25-2Upstream product

14404-25-2Downstream Products

14404-25-2Relevant articles and documents

Acetylacetoneacetylacetonetriphenyl phosphine carbonyl and rhodium synthesis process

-

Paragraph 0028; 0029; 0030, (2017/08/29)

An acetylacetonetriphenyl phosphine carbonyl and rhodium synthesis process comprises the following steps: 1, heating a rhodium chloride trihydrate crystalline powder material at an atmosphere of carbon monoxide, until gradual reaction, sublimation, condensation, and gradual generation of orange red needle crystals, i.e., tetracarbonyl dichloride; 2, based on weight by parts, dissolving a mixture of 2-3 parts of tetracarbonyl dichloride, 5-7 parts of acetylacetone, and 7-9 parts of barium carbonate into 125-135 parts of petroleum ether, heating reflux for a week, and then cooling and filtering; evaporating the filtered liquid to remove the solution so as to obtain crystal having dichroism of red and green, i.e., acetylacetone carbonyl and rhodium; and 3, dropping a benzene solution of acetylacetone carbonyl and rhodium slowly into a benzene solution of triphenyl phosphine, filtering the reaction liquid when carbon monoxide bubbles are no longer generated, and washing a filter cake with sufficient diethyl ether to obtain yellow microcrystal, i.e., acetylacetonetriphenyl phosphine carbonyl and rhodium.

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