Scholarly article on 4-ethoxy-1-(2-phenyl-thiazol-4-yl)-butan-1-one 21917-78-2 from Journal of the Chemical Society C: Organic p. 707 - 710

DOI: 10.1039/j39690000707

Source and publish data:

Journal of the Chemical Society C: Organic p. 707 - 710 (1969)

Update date:2022-08-15

Topics:

Authors:

Jones,D.G.

Jones,G.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1039/j39690000707

Full text of DOI:10.1039/j39690000707

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:4-ethoxy-1-(2-phenyl-thiazol-4-yl)-butan-1-one

Cas No:21917-78-2

R&D Labs maybe for 21917-78-2

Xuzhou Tianrun Chemical Co.,Ltd

website:http://www.tianrunchem.cn

Contact:86-516-83832636

Address:fuxing road
ChangZhou XiaQing Chemical Co., Ltd.

Contact:+86-519-88721665

Address:3# Hengluo Road, Henglin Town, Changzhou City, Jiangsu Province，China
C-LAB Chemievermittlung GmbH

Contact:+49-9398-993127

Address:Untertorstr. 27
AUSHUN PHARMACEUTICAL TECHNOLOGY CO,.LTD

Contact:+86-25-86883560 15951806178

Address:14 Dayingbi, Zhujiang Rd. East, Nanjing, Jiangsu, China.
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA

Relevant to this article

Conformationally constrained analogues of diacylglycerol. 11.¹ Ultrapotent protein kinase C ligands based on a chiral 5-disubstituted tetrahydro-2-furanone template

Doi:10.1021/jm950277n
(1996)
Regio- and Enantioselective Ni-Catalyzed Formal Hydroalkylation, Hydrobenzylation, and Hydropropargylation of Acrylamides to α-Tertiary Amides

Doi:10.1002/anie.202011339
(2021)
5-aza-7-deazaguanine DNA: Recognition and strand orientation of oligonucleotides incorporating anomeric imidazo[1,2-α]-1,3,5-triazine nucleosides

Doi:10.1002/1522-2675(20010711)84:7<1996::AID-HLCA1996>3.0.CO;2-1
(2001)
Doi:10.1039/j29690000192
(1969)
Doi:10.1007/BF00481038
()
β-enaminoesters as building blocks in heterocyclic synthesis. A novel synthesis of fused azines by using biaise reaction as a key step

Doi:10.1002/(SICI)1521-3897(199902)341:2<147::AID-PRAC147>3.0.CO;2-I
(1999)

Article Doi

DOI: 10.1039/j39690000707