729590-57-2 Usage
Description
4-Benzyloxy-1-bromo-2-chloro-benzene is an organic compound with the chemical formula C13H10BrClO. It is a benzene derivative featuring a bromo and chloro substituent, as well as a benzyloxy group. 4-Benzyloxy-1-broMo-2-chloro-benzene is known for its role as an intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
4-Benzyloxy-1-bromo-2-chloro-benzene serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Benzyloxy-1-bromo-2-chloro-benzene is utilized as an intermediate for the production of pesticides and other agrochemicals. Its presence in these compounds can enhance their effectiveness in agricultural applications.
Used in Organic Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, 4-Benzyloxy-1-bromo-2-chloro-benzene also acts as a versatile building block in the synthesis of a wide range of chemical compounds. Its reactivity and structural features make it valuable in creating new organic molecules for various purposes.
It is important to handle and store 4-Benzyloxy-1-bromo-2-chloro-benzene under controlled conditions due to its potential hazards and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 729590-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,9 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 729590-57:
(8*7)+(7*2)+(6*9)+(5*5)+(4*9)+(3*0)+(2*5)+(1*7)=202
202 % 10 = 2
So 729590-57-2 is a valid CAS Registry Number.
729590-57-2Relevant articles and documents
A re-investigation of the Fries rearrangement of 3-chlorophenyl acetate and synthesis of 2-azido-1-(4-(benzyloxy)-2-chlorophenyl)ethanone from 4-bromo-3-chlorophenol
Procopiou, Panayiotis A.,Coe, Diane M.,Procopiou, George
, p. 4766 - 4768 (2017/11/20)
The Fries rearrangement of 3-chlorophenyl acetate provided the expected 4-chloro-2-hydroxy-acetophenone as the major product and 2,4-diacetyl resorcinol and 2-chloro-4-hydroxy-acetophenone as minor products. 4-Benzyloxy-2-chloroacetophenone was prepared by a Heck reaction and then elaborated to 4-benzyloxy-2-chlorophenacyl azide.
SUBSTITUTED CYCLOPROPYL COMPOUNDS USEFUL AS GPR119 AGONISTS
-
Page/Page column 54, (2013/06/05)
Substituted cyclopropyl compounds of the formula (I): and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-119. Pharmaceutical compositions and methods of treatment are also included
CYCLIC AMINOPHENYL SULFAMATE DERIVATIVE
-
Page/Page column 29, (2010/11/08)
This invention provides cyclicamino-phenyl sulfamate derivatives represented by a formula wherein each of R1 and R2 stands for hydrogen or lower alkyl; each of R3 and R4 stands for hydrogen, halogen, cyano or the like; A stands for nitrogen or CH; B stands for CH2, SO2, CO, optionally substituted phenyl or the like; and R5 stands for alkyl, phenyl, amino or the like, or salts thereof which exhibit excellent steroid sulfatase inhibitory activity and are useful for prevention or treatment of diseases associated with steroids such as estrogen, androgen and the like.
