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2H-Pyran-2-one, 5,6-dihydro-6-[(1Z)-2-phenylethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

389796-50-3

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389796-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389796-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,7,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 389796-50:
(8*3)+(7*8)+(6*9)+(5*7)+(4*9)+(3*6)+(2*5)+(1*0)=233
233 % 10 = 3
So 389796-50-3 is a valid CAS Registry Number.

389796-50-3SDS

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 Z-goniothalamin

1.2 Other means of identification

Product number -
Other names goniothalamin

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:389796-50-3 SDS

389796-50-3Relevant academic research and scientific papers

Annulation-retro-Claisen cascade of bifunctional peroxides for the synthesis of lactone natural products

Hu, Lin,Li, Jialin,Li, Xuemin,Xu, Qianlan

supporting information, p. 274 - 277 (2022/01/03)

A new and highly efficient annulation-retro-Claisen cascade, which involves the [4 + 1] or [5 + 1] annulation of α-benzoylacetates with bielectrophilic peroxides and a subsequent debenzoylation process under mild basic conditions, has been developed for the rapid construction of valuable tetrahydrofuran- and dihydropyran-2-carboxylates in good yields. By employing the new reaction, the unified total synthesis of γ- and δ-lactone natural products such as (±)-tanikolide, (±)-goniothalamins, (±)-7-epi-goniodiol, and (±)-plakolide A has been accomplished in 4-7 steps.

Design, synthesis, in vitro cytotoxicity evaluation and structure-activity relationship of Goniothalamin analogs

Mohideen, Mazlin,Zulkepli, Suraya,Nik-Salleh, Nik-Salmah,Zulkefeli, Mohd,Weber, Jean-Frédéric Faizal Abdullah,Rahman, A. F. M. Motiur

, p. 812 - 831 (2013/07/26)

A series of six/five member (E/Z)-Goniothalamin analogs were synthesized from commercially available (3,4-dihydro-2H-pyran-2-yl)methanol/5- (hydroxymethyl)dihydrofuran-2(3H)-one in three steps with good to moderate overall yields and their cytotoxicity against lymphoblastic leukemic T cell line (Jurkat E6.1) have been evaluated. Among the synthesized analogs, (Z)-Goniothalamin appeared to be the most active in cytotoxicity (IC 50 = 12 μM). Structure-activity relationship study indicates that introducing substituent in phenyl ring or replacing phenyl ring by pyridine/naphthalene, or decreasing the ring size of lactones (from six to five member) do not increase the cytotoxicity.

Gold-catalyzed intermolecular reactions of propiolic acids with alkenes: [4 + 2] Annulation and enyne cross metathesis

Yeom, Hyun-Suk,Koo, Jaeyoung,Park, Hyun-Sub,Wang, Yi,Liang, Yong,Yu, Zhi-Xiang,Shin, Seunghoon

supporting information; experimental part, p. 208 - 211 (2012/02/16)

A gold-catalyzed intermolecular reaction of propiolic acids with alkenes led to a [4 + 2] annulation or enyne cross metathesis. The [4 + 2] annulation proceeds with net cis-addition with respect to alkenes and provides an expedient route to α,β-unsaturate

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