Cas 1340599-26-9,methyl 2-(4-nitrophenyl)thiazole-4-carboxylate

1340599-26-9

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Basic information

Product Name: methyl 2-(4-nitrophenyl)thiazole-4-carboxylate
Synonyms: methyl 2-(4-nitrophenyl)thiazole-4-carboxylate
CAS NO:1340599-26-9
Molecular Formula:
Molecular Weight: 264.262
EINECS: N/A
Product Categories: N/A

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: methyl 2-(4-nitrophenyl)thiazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(4-nitrophenyl)thiazole-4-carboxylate(1340599-26-9)
EPA Substance Registry System: methyl 2-(4-nitrophenyl)thiazole-4-carboxylate(1340599-26-9)

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: 1340599-26-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1340599-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,0,5,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1340599-26:
(9*1)+(8*3)+(7*4)+(6*0)+(5*5)+(4*9)+(3*9)+(2*2)+(1*6)=159
159 % 10 = 9
So 1340599-26-9 is a valid CAS Registry Number.

1340599-26-9Upstream product

1340599-26-9Downstream Products

1340599-26-9Relevant academic research and scientific papers

The Synthesis and Biological Evaluation of Anithiactin A/Thiasporine C and Analogues

Lamb, Richard A.,Badart, Michael P.,Swaney, Brooke E.,Gai, Sinan,Baird, Sarah K.,Hawkins, Bill C.

, p. 1829 - 1833 (2015)

The synthesis of anithiactin A has been achieved in four steps. Several closely related analogues were synthesised and their biological activity against colon and breast cancer cell lines evaluated. Anithiactin A was found not to be cytotoxic even at a hi

Concise synthesis of 2,4-disubstituted thiazoles from β-azido disulfides and carboxylic acids or anhydrides: Asymmetric synthesis of cystothiazole C

Liu, Yi,Sun, Xue,Zhang, Xing,Liu, Jun,Du, Yuguo

, p. 8453 - 8461 (2014/12/10)

A novel and efficient method for the one-pot synthesis of 2,4-disubstituted thiazoles from carboxylic acids or anhydrides is presented. Based on this new method, the total synthesis of the bis-2,4-disubstituted bis(thiazoles) natural product cystothiazole C is also presented. This journal is

Convenient Synthesis of Azolines to Azoles

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Paragraph 0102; 0105, (2013/03/26)

Azolines are oxidized in the presence of a copper-containing catalyst to azoles in the presence of molecular oxygen. A synthetic scheme converting azolines azoles is also provided.

Copper-catalyzed oxidation of azolines to azoles

Dawsey, Anna C.,Li, Vincent,Hamilton, Kimberly C.,Wang, Jianmei,Williams, Travis J.

, p. 7994 - 8002 (2012/08/08)

We report herein convenient, aerobic conditions for the oxidation of thiazolines to thiazoles and data regarding the oxidation mechanism. These reactions feature operationally simple and environmentally benign conditions and proceed in good yield to afford the corresponding azoles, thus enabling the inexpensive preparation of valuable molecular building blocks. Incorporation of a novel diimine-ligated copper catalyst, [(MesDABMe) CuII(OH2)3]2+ [-OTf] 2, provides increased reaction efficiency in many cases. In other cases copper-free conditions involving a stoichiometric quantity of base affords superior results.

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