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1H-Indole, 6-bromo-4-(phenylmethoxy)-, also known as 4-(Benzyloxy)-6-bromo-1H-indole, is an organic compound that serves as a key reactant in the synthesis of various chemical compounds. It is characterized by the presence of an indole ring, a bromine atom at the 6th position, and a phenylmethoxy group at the 4th position. This unique structure makes it a valuable intermediate in the production of pharmaceuticals and other organic compounds.

1070503-92-2

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1070503-92-2 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indole, 6-bromo-4-(phenylmethoxy)is used as a reactant in the synthesis of IDO inhibitors, such as exiguamine A and B. These inhibitors are of significant interest in the pharmaceutical industry due to their potential applications in the treatment of various diseases, including cancer and inflammatory disorders. The indole-based structure of 1H-Indole, 6-bromo-4-(phenylmethoxy)- allows for the development of novel and effective inhibitors targeting the IDO enzyme, which plays a crucial role in immune response and has been implicated in the pathogenesis of several diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1070503-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,5,0 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1070503-92:
(9*1)+(8*0)+(7*7)+(6*0)+(5*5)+(4*0)+(3*3)+(2*9)+(1*2)=112
112 % 10 = 2
So 1070503-92-2 is a valid CAS Registry Number.

1070503-92-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-4-phenylmethoxy-1H-indole

1.2 Other means of identification

Product number -
Other names W-1263

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1070503-92-2 SDS

1070503-92-2Relevant academic research and scientific papers

Total synthesis of exiguamines A and B inspired by catecholamine chemistry

Sofiyev, Vladimir,Lumb, Jean-Philip,Volgraf, Matthew,Trauner, Dirk

, p. 4999 - 5005 (2012/06/04)

The evolution of a total synthesis of the exiguamines, two structurally unusual natural products that are highly active inhibitors of indolamine-2,3-dioxygenase (IDO), is described. The ultimately successful strategy involves advanced cross-coupling methodology and features a potentially biosynthetic tautomerization/electrocyclization cascade reaction that forms two heterocycles and installs a quaternary ammonium ion in a single synthetic operation. Copyright

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