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20412-62-8

20412-62-8

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20412-62-8 Usage

Chemical Properties

light yellow to beige powder

Check Digit Verification of cas no

The CAS Registry Mumber 20412-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,1 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20412-62:
(7*2)+(6*0)+(5*4)+(4*1)+(3*2)+(2*6)+(1*2)=58
58 % 10 = 8
So 20412-62-8 is a valid CAS Registry Number.

20412-62-8 Well-known Company Product Price

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  • Aldrich

  • (164100)  Ethylacetoacetatesodiumsalt  

  • 20412-62-8

  • 164100-50G

  • 707.85CNY

  • Detail

20412-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL ACETOACETATE SODIUM SALT

1.2 Other means of identification

Product number -
Other names 2-ETHYLACETOACETIC ACID

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:20412-62-8 SDS

20412-62-8Upstream product

20412-62-8Relevant articles and documents

Photocatalytic ?±-oxyamination of stable enolates, silyl enol ethers, and 2-oxoalkane phosphonic esters

Schroll, Peter,K??nig, Burkhard

supporting information, p. 309 - 313 (2015/03/03)

Fast ?±-oxyamination of stable enolates, silyl enol ethers, and in situ deprotonated dialkyl 2-oxoalkane phosphonates and diphenyl-2-oxoalkyl phosphine oxides was performed in the presence of [Ru(bpy)3]2+ (bpy = 2,2a?2-bipyridyl) as a photocatalyst, 2,2,6,6-tetramethylpiperidine nitroxide (TEMPO), and visible light. The key step was the light-induced one-electron oxidation of TEMPO into the 2,2,6,6-tetramethylpiperidine- 1-oxoammonium ion, which was nucleophilically attacked to yield ?±-functionalized carbonyl compounds. The reaction time was significantly reduced by the use of the microreactor flow technique.

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