Scholarly article on 4-Methylnonanal-2,4-dinitro-phenylhydrazon 22250-85-7 from Journal of the American Chemical Society p. 731 - 737

DOI: 10.1021/ja01031a039

Source and publish data:

Journal of the American Chemical Society p. 731 - 737 (1969)

Update date:2022-07-29

Topics:

Authors:

Snyder,C.D.

Rapoport,H.

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

Article abstract of DOI:10.1021/ja01031a039

Full text of DOI:10.1021/ja01031a039

Products guided by the article

Product name:4-Methylnonanal-2,4-dinitro-phenylhydrazon

Cas No:22250-85-7

R&D Labs maybe for 22250-85-7

Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
Shijiazhuang Frontierchem Co., Ltd.

Contact:+86-311-89271196

Address:4-4-202 No.15 Biandian Street,Shijiazhuang
Jiangxi Province Bethel Pharmaceutical Co., Ltd.

Contact:+86-795-259 3456 ，+86-15957688008 13566650571

Address:Huangjindui Chemical Park， Shanggao County ，Yichun city，Jiangxi Province
Huayang chemical Co., LTD

Contact:+86-18653358619

Address:zibo

Relevant to this article

Regioselective Radical Cyclization by Electrochemical Reduction Using an Arene Mediator. Environmentally Benign Method

Doi:10.1246/cl.2003.720
(2003)
Unusual [1,2]- and [1,3]-M(CO)₅ shifts in Fischer carbene complexes: [4 + 3] and [3 + 3] annulation reactions of furan and pyrrole rings

Doi:10.1021/ja983692o
(1999)
Systematic synthesis of specifically ¹³C/²H-labeled nucleosides from [ul-¹³C₆]-D-glucose

Doi:10.1016/S0040-4039(98)00432-8
(1998)
Synthesis of the South unit of cephalostatin. 7. Total syntheses of (+)- cephalostatin 7, (+)-cephalostatin 12, and (+)-ritterazine K

Doi:10.1021/ja9817141
(1999)
Synthesis of a hydroxylated muricatacin analog related to squamocin

Doi:10.1016/S0040-4039(99)00127-6
(1999)
Flat peptides

Doi:10.1021/ja9842114
(1999)

Article Doi

DOI: 10.1021/ja01031a039