FORMATION OF 4-NITROSOQUINOLINE 1-OXIDE AND SYNTHESIS OF

DOI: 10.1248/yakushi1947.85.1_69

Source and publish data:

Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 69 - 71 (1965)

Update date:2022-07-29

Topics:

Authors:

KOSUGE KOSUGE

YOKOTA YOKOTA

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

Article abstract of DOI:10.1248/yakushi1947.85.1_69

Full text of DOI:10.1248/yakushi1947.85.1_69

Products guided by the article

Product name:4-phenylazo-quinoline-1-oxide

Cas No:1150-97-6

R&D Labs maybe for 1150-97-6

Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China
Molobelamltrading

Contact:27-792-602929

Address:SIDNEY MUFAMADI STREET 009949 X44 0700 POLOKWANE,LIMPOPO
Daicel Chiral Technologies (China)CO.,LTD

Contact:021-5046-0086*8

Address:Part C, FL 5, the 16th Building, No. 69, XiYa Road, WaiGaoQiao Free Trade Zone, Shanghai, 200131, P.R.China
Zouping Fuhai Technology Development Co., Ltd.

Contact:+0532-86934525 18660293207

Address:jiuhu town industrial park Zouping County,bingzhou Provincejiuhu town industrial park
Xi'an Costrong Pharmaceutical Co., Ltd.

Contact:029- 68576496

Address:Room 2004,Shuibao Building,No.190,South Erhuan Rd, Yanta District,Xi'an,Shaan Xi,China

Relevant to this article

Metalation of Phenols. Synthesis of Benzoquinones by the Oxidative Degradation Approach

Doi:10.1021/jo00253a019
(1988)
Ordered Mesoporous CeO₂-supported Ag as an Effective Catalyst for Carboxylative Coupling Reaction Using CO₂

Doi:10.1002/cctc.201900039
(2019)
Total synthesis of incednam, the aglycon of incednine

Doi:10.1021/ol102400c
(2010)
Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents

Doi:10.1016/j.ejmech.2008.10.011
(2009)
Electrophilic ipso-halocyclization of N-arylpropynamides with polyfluoroalkyl alcohols: Selective synthesis of 8-(polyfluoroalkoxy)azaspiro[4. 5]trienes

Doi:10.1055/s-0028-1087972
(2009)
Doi:10.1021/jo01363a616
(1957)

Article Doi