tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate, 97%
tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate, 97%
tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate, 97%
Thermo Scientific Chemicals

tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate, 97%

CAS: 114772-40-6 | C18H19BrO2 | 347.252 g/mol
製品番号(カタログ番号) H54100.06
または、製品番号H54100-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
仕様
CAS114772-40-6
化学物質名または材質tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate
EINECS番号442-850-9
式量347.24
健康被害1H317
さらに表示
1,1-Dimethylethyl Esterbiphenyl is used in the preparation of angiotensin II receptor antagonists.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,1-Dimethylethyl Esterbiphenyl is used in the preparation of angiotensin II receptor antagonists.

Solubility
Soluble in chloroform, ethyl acetate, and DMSO.

Notes
Store in a cool, dry place, in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. David P. Marciano; Dana S. Kuruvilla; Siddaraju V. Boregowda; Alice Asteian; Travis S. Hughes; Ruben Garcia-Ordonez; Cesar A. Corzo; Tanya M. Khan; Scott J. Novick; HaJeung Park; Douglas J. Kojetin; Donald G. Phinney; John B. Bruning; Theodore M. Kamenecka & Patrick R. Griffin. Pharmacological repression of PPARγ promotes osteogenesis. Nature Communications. 2015, 6.
  2. Masood Hosseini; Longguang Jiang; Hans Peter Sørensen; Jan K. Jensen; Anni Christensen; Sarah Fogh; Cai Yuan; Lisbeth M. Andersen; Mingdong Huang; Peter A. Andreasen and Knud J. Jensen. Elucidation of the Contribution of Active Site and Exosite Interactions to Affinity and Specificity of Peptidylic Serine Protease Inhibitors Using Non-Natural Arginine Analogs. Molecular Pharmacology. 2009, 80 (4), 585-597.