Benzyl 2--2-phenylacetate and its α-Amino Acid

DOI: 10.1107/S0108270194002829

Source and publish data:

Acta Crystallographica, Section C: Crystal Structure Communications p. 1604 - 1608 (1994)

Update date:2022-08-04

Topics:

Authors:

Urtiaga, Miren Karmele

Arriortua, Maria Isabel

Badia, Dolores

Dominguez, Esther

Maria, Anna

et al. et al.

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

Article abstract of DOI:10.1107/S0108270194002829

The structures of benzyl 2--2-phenylacetate, C29H27NO4S, (I), and 2--2-phenylacetic acid, C22H21NO4S, (II), have been determined.The geometries of both compounds are similar.The N a

Full text of DOI:10.1107/S0108270194002829

Products guided by the article

Product name:DL-benzyl 2--2-phenylacetate

Cas No:159831-04-6

R&D Labs maybe for 159831-04-6

Onlychem (Jinan)Biotech Co.,Ltd

Contact:86-531-83175885

Address:No. 44, Honglou South Road, Jinan,China
Qingdao S. H. Huanyu Imp. & Exp. Co., Ltd.

Contact:86-532-88250866

Address:Room 615, World Trade Centre Building B, Hongkong Middle Roda 6#, Qingdao, Shandong, China
Skyrun Industrial Co.,Ltd(expird)

website:http://www.chinaskyrun.com

Contact:0086-576-84610586

Address:Chemical Development Zone
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District
Zhejiang PRIMAR Import & Export Trade Co., Ltd.

Contact:86-570-3630818

Address:No.1Puzhuyuan,Quhua,Zhejiang Province,China324004

Relevant to this article

Synthesis of Zirconium Phosphonate Supported L -Proline as an Effective Organocatalyst for Direct Asymmetric Aldol Addition

Doi:10.1002/ejoc.201301673
(2014)
Potassium phthalimide-N-oxyl: A novel, efficient, and simple organocatalyst for the one-pot three-component synthesis of various 2-amino-4H-chromene derivatives in water

Doi:10.1016/j.tet.2012.11.068
(2013)
Microwave synthesis and anticonvulsant activity of 2-benzyl- 1(2H)-phthalazinones

Doi:10.1002/jhet.5570360444
(1999)
Discovery of 3,3′-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection

Doi:10.1021/acsmedchemlett.7b00418
(2018)
Catalytic Enantioselective Double Carbopalladation/C?H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach

Doi:10.1002/anie.201709133
(2017)
Synthesis of 3-alkoxy-3-aryl-4,4-diisopropyl-1,2-dioxetanes and their base-induced chemiluminescence

Doi:10.1016/S0040-4020(99)00124-6
(1999)

Article Doi