Scholarly article on phenyl 2,4-dihydroxybenzoate 16700-99-5 from Journal of the American Chemical Society p. 3237 - 3248

DOI: 10.1021/ja00742a024

Source and publish data:

Journal of the American Chemical Society p. 3237 - 3248 (1971)

Update date:2022-08-02

Topics:

Authors:

Maugh,T.

Bruice,T.C.

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

Article abstract of DOI:10.1021/ja00742a024

Full text of DOI:10.1021/ja00742a024

Products guided by the article

Product name:phenyl 2,4-dihydroxybenzoate

Cas No:16700-99-5

R&D Labs maybe for 16700-99-5

Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796909136--

Address:No 18 Guoqiao Road
Zhejiang Genebest Pharmaceutical Co.,Ltd.

Contact:0086-571-63532866

Address:No.1 Jinboshi Rd Lishan Town Fuyang City Zhejiang Province China
Advanced Biotech

Contact:+1-973-357-0577

Address:10 Taft Rd.
Taizhou YOJOY Chemical Co., Ltd.

Contact:13857143241

Address:Yangfu Industrial Park, Xianju, Zhejiang, P. R. China
Exploiter Molybdenum Co.,Ltd

Contact:86-379-63338609

Address:Jiudian Village,Deting Town,Song County,Luoyang

Relevant to this article

Reaction of with Phenylacetylene. A Novel Type of Alkylidyne-Alkyne Coupling in a Triosmium Alkylidyne Cluster

Doi:10.1039/DT9950001497
(1995)
Synthesis of (+/-)-<4aα,4bβ,10bβ,12aβ>-9-halogeno-2-methyl-1,2,3,4,4a,5,6,10b,11,12,12a-dodecahydronaphtho<2,1-f>isoquinolines

Doi:10.1039/P19950001273
(1995)
Doi:10.1007/BF00909621
()
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues

Doi:10.1021/jm990095j
(1999)
Hypervalent bond formation in halogeno(2-acylphenyl)bismuthanes

Doi:10.1021/om00008a036
(1995)
Novel 1,3,4-thiadiazole conjugates derived from protocatechuic acid: Synthesis, antioxidant activity, and computational and electrochemical studies

Doi:10.1016/j.crci.2019.06.001
(2019)

Article Doi

DOI: 10.1021/ja00742a024

Source and publish data: