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(Z)-6-chloro-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32781-14-9

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32781-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32781-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32781-14:
(7*3)+(6*2)+(5*7)+(4*8)+(3*1)+(2*1)+(1*4)=109
109 % 10 = 9
So 32781-14-9 is a valid CAS Registry Number.

32781-14-9Relevant academic research and scientific papers

“On water” ultrasound-assisted one pot efficient synthesis of functionalized 2-oxo-benzo[1,4]oxazines: First application to the synthesis of anticancer indole alkaloid, Cephalandole A

Jaiswal, Pradeep K.,Sharma, Vashundhra,Prikhodko, Jaroslav,Mashevskaya, Irina V.,Chaudhary, Sandeep

, p. 2077 - 2083 (2017)

For the first time, an efficient, simple, synthetic green protocol for the one-pot synthesis of functionalized 2-oxo-benzo[1,4]oxazines 24–29 in water under ultrasound irradiation is presented. As compared to conventional methods, the present protocol avo

Non-peptide-based new class of platelet aggregation inhibitors: Design, synthesis, bioevaluation, SAR, and in silico studies

Jaiswal, Pradeep K.,Sharma, Vashundhra,Kumar, Surendra,Mathur, Manas,Swami, Ajit K.,Yadav, Dharmendra K.,Chaudhary, Sandeep

, (2018/03/21)

A series of 2-oxo-2-phenylethylidene linked 2-oxo-benzo[1,4]oxazine analogues 17a–x and 18a–o, incorporated with a variety of electron-withdrawing as well as electron-donating groups at ring A and ring C, were synthesized under greener conditions in excel

Five-membered 2,3-dioxo heterocycles: XCVIII.* [4 + 2]-cycloaddition of alkyl vinyl ethers to 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4- triones. A new synthetic approach to heteroanalogs of 13(14→8)-abeo steroids

Stepanova,Aliev,Maslivets

, p. 1762 - 1767 (2014/08/05)

3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones reacted with alkyl vinyl ethers according to the [4 + 2]-cycloaddition pattern with formation of substituted (1S*,16R*)- and (1R*,16R*)-16-alkoxy-14- aryl-3,15-dioxa-10-azatetracyclo[8.7.0.01,13.04,9

Five-membered 2,3-dioxo heterocycles: LXXVII. [4 + 2]-cycloaddition of alkyl vinyl ethers to 3-aroylpyrrolo[2,1-c][1,4]benzoxazine-1,2,4(4H)-triones

Stepanova,Babenysheva,Maslivets

experimental part, p. 937 - 940 (2011/10/09)

[4 + 2]-Cycloaddition of 3-aroylpyrrolo[2,1-c][1,4]benzoxazine-1,2,4(4H)- triones to alkyl vinyl ethers gave substituted stereoisomeric (1R,16R)- and (1S,16R*)-16-alkoxy-14-aryl-3,15-dioxa-10-azatetracyclo[ 8.7.0.0 1,13.04,9]heptadec

Chemistry of acyl(imidoyl)ketenes: IX. Synthesis and thermolysis of 3-aroyl-8-chloro-1,2-dihydro-4H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones

Semenova,Krasnykh

, p. 1222 - 1227 (2007/10/03)

Reactions of 3-Z-aroylmethylene-6-chloro-3,4-dihydro-2H-1,4-benzoxazine-2- ones with oxalyl chloride afford 3-aroyl-8-chloro-1,2-dihydro-4H-pyrrolo[2,1-c] [1,4]benzoxazine-1,2,4-triones and Z-3-(2-aryl-2-chlorovinyl)-6-chloro-2H-1,4- benzoxazine-2-ones. A

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