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

taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
Jiangsu Taihu New Materials Holding Co., Ltd

Contact:+86-519-86160108

Address:Xueyan Town, Changzhou City, Jiangsu Province, 213169, China
TIANJIN GST CHEMICAL TECHNOLOGY CO., LTD

Contact:+86-22-25210964

Address:Room. 208, No. -12-C, No. 13, Xinbei Road, Tanggu District, New Haixin Area, Tianjin City, China
Dragon Chemical Co., Ltd.

Contact:0571-

Address:zhejing
Henan Techway Chemical Co.,Ltd.

website:http://www.techwaychem.com

Contact:+86-371-66380080

Address:No.27 Shunhe Road,

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