Scholarly article on 4-Acetylpyridine 1122-54-9 from Journal of Magnetic Resonance (1969) p. 69,70,72

DOI: 10.1016/0022-2364(78)90171-3

Source and publish data:

Journal of Magnetic Resonance (1969) p. 69,70,72 (1978)

Update date:2022-08-17

Topics:

Authors:

Dohrmann

Kieslich

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

Article abstract of DOI:10.1016/0022-2364(78)90171-3

Full text of DOI:10.1016/0022-2364(78)90171-3

Products guided by the article

Product name:4-Acetylpyridine

Cas No:1122-54-9

R&D Labs maybe for 1122-54-9

WUHAN RISON TRADING CO.,LTD

Contact:0086-27-83607103/83642615

Address:No.498, Jianshe Ave, Wuhan, China
Suzhou Health Chemicals Co., Ltd.

website:http://www.healthchems.com

Contact:13776257979

Address:No. 338, Jingang Avenue,
Guangzhou Probig Fine Chemical Co., Ltd.

Contact:020-86297874

Address:No.2, 1/F, No.20, Hetai Road,Hebian Village, Baiyun District,Guangzhou,China
Huaihua Baohua Biotechnology Co.,Ltd

website:http://www.baochengchem.com

Contact:86-519-82698291

Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
Jiangsu Allyrise Pharmaceutical Co., Ltd.(expird)

Contact:+86-523-86818997

Address:Taizhou,Jiangsu Province,CHINA

Relevant to this article

Copper-Catalyzed 1,6-Hydrodifluoroacetylation of para-Quinone Methides at Ambient Temperature with Bis(pinacolato)diboron as Reductant

Doi:10.1002/adsc.201600991
(2017)
Cinnamomum tamala leaf extract-mediated green synthesis of Ag nanoparticles and their use in pyranopyrazles synthesis

Doi:10.1016/S1872-2067(15)60853-1
(2015)
Doi:10.1039/CT9232301826
(1923)
Comparison of electron spin relaxation times measured by Carr-Purcell-Meiboom-Gill and two-pulse spin-echo sequences

Doi:10.1016/S1090-7807(03)00182-4
(2003)
Synthesis of β-Trifluoromethylated Alkyl Azides via a Manganese-Catalyzed Trifluoromethylazidation of Alkenes with CF₃SO₂Na and TMSN₃

Doi:10.1002/adsc.201800488
(2018)
Teaming up synthetic chemistry and histochemistry for activity screening in galectin-directed inhibitor design

Doi:10.1007/s00418-016-1525-5
(2017)

Article Doi

DOI: 10.1016/0022-2364(78)90171-3