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1,5-Pentanedione, 2-methyl-1,3,5-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10226-00-3

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10226-00-3 Usage

Physical State

Yellow crystalline solid

Uses

a. Flavoring agent in the food industry
b. Pharmaceutical industry
c. Perfumes
d. Synthetic intermediate in organic chemistry

Safety

Relatively safe compound

Potential Hazards

Can be irritating to skin and eyes in high concentrations

Handling Precautions

Handle with care and store in a well-ventilated area

Check Digit Verification of cas no

The CAS Registry Mumber 10226-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10226-00:
(7*1)+(6*0)+(5*2)+(4*2)+(3*6)+(2*0)+(1*0)=43
43 % 10 = 3
So 10226-00-3 is a valid CAS Registry Number.

10226-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1,3,5-triphenyl-pentane-1,5-dione

1.2 Other means of identification

Product number -
Other names α.ε-Dioxo-β-methyl-α.γ.ε-triphenyl-pentan

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:10226-00-3 SDS

10226-00-3Relevant academic research and scientific papers

Lithium acetate-catalyzed Michael reaction between trimethylsilyl enolate and α,β-unsaturated carbonyl compound

Nakagawa, Takashi,Fujisawa, Hidehiko,Nagata, Yuzo,Mukaiyama, Teruaki

, p. 1016 - 1017 (2004)

Lithium acetate-catalyzed Michael reaction between trimethylsilyl enolates and α,β-unsaturated carbonyl compounds in DMF proceeded smoothly to afford the corresponding Michael-adducts in good to high yields. Hindered α,β-unsaturated ketones also behaved as an excellent Michael-acceptor in the above reaction at room temperature.

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