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

Nanjing Fayekong Chemcial Co.,Ltd(expird)

Contact:86-25-58813444

Address:Rm 1503, Unit 1, Building 5, Zijinnanyuan, Nanjing, Jiangsu, China
ZHEJIANG JIANYE CHEMICAL CO.,LTD.

Contact:86-571-64149273,64149234

Address:No. 48, Fuxi Road, Meicheng Town
Shanghai Forever Biotech Co., Ltd.

Contact:+86-21-69734790

Address:Room 5017/5019、5022、5024 of Technology Innovation Centre, No.1155, Gongyuan East Rd, QingPu District, Shanghai China.
Huangshi Meifeng Chemical Co.,ltd.

Contact:+86-714-6516706

Address:1941-4-3#,Hubin Avenue,Huangshi,Hubei,China
Purestar Chem Enterprise Co.,Ltd

website:http://www.purestarchem.com

Contact:05722157374

Address:no235.huanchengdong Rd

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