Scholarly article on 3,5-Dinitro-benzoesaeure-2-isobutenyl-phenylester 107151-75-7 from Journal of the American Chemical Society p. 3662,3665

DOI: 10.1021/ja01499a048

Source and publish data:

Journal of the American Chemical Society p. 3662,3665 (1960)

Update date:2022-07-30

Topics:

Authors:

Hurd Hurd

Dowbenko

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

Article abstract of DOI:10.1021/ja01499a048

Full text of DOI:10.1021/ja01499a048

Products guided by the article

Product name:3,5-Dinitro-benzoesaeure-2-isobutenyl-phenylester

Cas No:107151-75-7

R&D Labs maybe for 107151-75-7

Suzhou Tianma Specialty Chemicals Co.,Ltd

Contact:+86-512-68090577

Address:#199, Huayuan Rd, Mudu, Suzhou, Jiangsu, CHINA
Huangshi Shennong Chemical Technology Co., Ltd

Contact:+86-714-3072290

Address:Eastern industrial park , Tieshan district , Huangshi city ,Hubei province , China
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing
Zibo Ocean International Trade Co.,Ltd(expird)

Contact:+86 533 5160706

Address:1117, Hongtai Bld., Songling rd, Zichuan,Zibo,Shandong,China
Chengdu Green technology Co.,Ltd.

Contact:86-28-82608355

Address:C9 ,Economic Headquarters, Economic Development Zone, Chengdu.

Relevant to this article

AROMATIC SOLVENT-INDUCED SHIFTS IN THE 1H-NMR SPECTRA OF NITRONES

Doi:10.1016/S0040-4020(01)88126-6
(1992)
Scalable synthesis of vicinal quaternary stereocenters via the solid-state photodecarbonylation of a crystalline hexasubstituted ketone

Doi:10.1021/acs.orglett.0c03226
(2020)
Ultrabright Terbium Nanoparticles for FRET Biosensing and in Situ Imaging of Epidermal Growth Factor Receptors**

Doi:10.1002/chem.202002007
(2020)
Synthesis, characterization, and photoluminescence of thiophene-containing spiro compounds

Doi:10.1055/s-2008-1078571
(2008)
Asymmetric synthesis of β-nitro ketones via Michael addition of lithiated α-amino nitriles to nitroalkenes

Doi:10.1021/jo8017318
(2008)
Design, synthesis, and structure-affinity relationships of novel series of sialosides as CD22-specific inhibitors

Doi:10.1021/jm8000696
(2008)

Article Doi

DOI: 10.1021/ja01499a048