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4H-1-Benzopyran-4-one, 6-methoxy-2-(2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84294-89-3

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84294-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84294-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84294-89:
(7*8)+(6*4)+(5*2)+(4*9)+(3*4)+(2*8)+(1*9)=163
163 % 10 = 3
So 84294-89-3 is a valid CAS Registry Number.

84294-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-2-(2-phenylethyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 6-methoxy-2-phenethylchromen-4-one

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:84294-89-3 SDS

84294-89-3Downstream Products

84294-89-3Relevant academic research and scientific papers

Synthesis of chiral chromanols: Via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones

Ma, Yujie,Li, Jing,Ye, Jianxun,Liu, Delong,Zhang, Wanbin

supporting information, p. 13571 - 13574 (2019/01/05)

Chiral chromanols and their derivatives have been synthesized via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones in high yields, >20:1 drs and with up to 99.9% ee. Control experiments show that the reaction undergoes two sequential asymmetric hydrogenation steps of the CC and CO double bonds. The reaction could be performed on a gram-scale with a relatively low catalyst loading (up to 1000 S/C), and the resulting products can be transformed to several biologically active compounds.

Synthesis of 2-(2-phenylethyl)chromones

Goel, Sharda,Shashi,Makrandi

, p. 535 - 536 (2007/10/03)

2-(2-Phenylethyl)chromones have been obtained by selective reduction of double bond of the styryl group in 2-styrylchromones involving catalytic hydrogen transfer reaction using ammonium formate in the presence of Pd-C.

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