Scholarly article on Trifluoroacetic acid o-tolyl ester 1736-10-3 from Journal of the American Chemical Society p. 2082,2084

DOI: 10.1021/ja01518a014

Source and publish data:

Journal of the American Chemical Society p. 2082,2084 (1959)

Update date:2022-08-11

Topics:

Authors:

Moffat Moffat

Hunt Hunt

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

Article abstract of DOI:10.1021/ja01518a014

Full text of DOI:10.1021/ja01518a014

Products guided by the article

Product name:Trifluoroacetic acid o-tolyl ester

Cas No:1736-10-3

R&D Labs maybe for 1736-10-3

Phytomarker Ltd.(expird)

Contact:+86-22-26358246

Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China
WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
SEA BRGIHT INDUSTRY CO.,LIMITED

Contact:0086 755 8622 3990

Address:Rm 17B3,GuangCaiXinTianDi Bldg,GuiMiao Rd,NanShan District,Shenzhen,China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:
Taizhou Green Peptide Trading Co., Ltd.

Contact:--

Address:Room 1501, No71, Yuehe Road, Taizhou City, Zhejiang Province, China

Relevant to this article

Doi:10.1039/c39720000884
(1972)
Studies on tridecaptin B₁, a lipopeptide with activity against multidrug resistant Gram-negative bacteria

Doi:10.1039/c5ob00780a
(2015)
Indium-Mediated Coupling of α-(Bromomethyl)acrylic Acid with Carbonyl Compounds in Aqueous Media. Concise Syntheses of (+)-3-Deoxy-D-glycero-D-galacto-nonulosonic Acid and N-Acetylneuraminic Acid

Doi:10.1021/jo00118a044
(1995)
Irreversible Inhibition of Mammalian and Insect Peptidylglycine &α-Hydroxylating Monooxygenases (PHMs), Peptide Amidating Enzymes, by N-Formyl Amides

Doi:10.1039/c39940001379
(1994)
Oxidation of sulfides with pyridinium tribromide in the presence of hydrated silica gel

Doi:10.1080/00397910600619044
(2006)
Pairing heterocyclic cations with closo-lcosahedral borane and carborane anions. i. benchtop aqueous synthesis of binary triazolium and imidazolium salts with limited water solubility

Doi:10.1021/ol900550v
(2009)

Article Doi

DOI: 10.1021/ja01518a014