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3-(2-hydroxy-5-methoxyphenyl)-1-phenyl-2-propene-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18288-07-8

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18288-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18288-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,8 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18288-07:
(7*1)+(6*8)+(5*2)+(4*8)+(3*8)+(2*0)+(1*7)=128
128 % 10 = 8
So 18288-07-8 is a valid CAS Registry Number.

18288-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-5-methoxy-chalcone

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-5-methoxy-chalkon

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:18288-07-8 SDS

18288-07-8Relevant academic research and scientific papers

Facile synthesis of 4H-chromene derivatives via base-mediated annulation of orffro-hydroxychalcones and 2-bromoallyl sulfones

Thadkapally, Srinivas,Kunjachan, Athira C.,Menon, Rajeev S.

, p. 16 - 21 (2016/04/05)

The cesium carbonate-mediated reaction of 2-bromoallyl sulfones and ortho-hydroxychalcones furnished 3-arylsulfonyl-4H-chromene derivatives in 58-67% yield (18 examples). 2-Bromoallyl sulfones functioned as synthetic surrogates for allenyl sulfones in the reaction.

Organocatalyzed michael-michael cascade reaction: Asymmetric synthesis of polysubstituted chromans

Jia, Zhen-Xin,Luo, Yong-Chun,Cheng, Xi-Na,Xu, Peng-Fei,Gu, Yu-Cheng

, p. 6488 - 6494 (2013/07/26)

An enantioselective cascade Michael-Michael reaction between chalcones enolates and nitromethane catalyzed by a bifunctional thiourea is developed. This reaction provides a mild but efficient approach to chiral benzopyrans bearing three consecutive stereocenters in high yields with excellent stereoselectivities, and the benzopyrans can be easily transformed to the corresponding tricyclic product.

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