Cas 939239-91-5,ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate

939239-91-5

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Basic information

Product Name: ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate
Synonyms: ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate
CAS NO:939239-91-5
Molecular Formula:
Molecular Weight: 307.327
EINECS: N/A
Product Categories: N/A
Mol File: 939239-91-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate(939239-91-5)
EPA Substance Registry System: ethyl 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetate(939239-91-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 939239-91-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 939239-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,2,3 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 939239-91:
(8*9)+(7*3)+(6*9)+(5*2)+(4*3)+(3*9)+(2*9)+(1*1)=215
215 % 10 = 5
So 939239-91-5 is a valid CAS Registry Number.

939239-91-5Upstream product

100-83-4 meta-hydroxybenzaldehyde

939239-91-5Downstream Products

503827-52-9 2-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetic acid

939239-91-5Relevant articles and documents

Design, synthesis, and activity evaluation of GK/PPARγ Dual-target-directed ligands as hypoglycemic agents

Lu, Jianxun,Lei, Lei,Huan, Yi,Li, Yongqiang,Zhang, Lijing,Shen, Zhufang,Hu, Wenxiang,Feng, Zhiqiang

, p. 922 - 927 (2014)

Based on the multi-target strategy to treat type 2 diabetes mellitus (T2DM), glucokinase/peroxisome proliferator-activated receptor γ (GK/PPARγ) dual-target molecules were constructed by the rational combination of pharmacophores from known GK activators

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