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13771-72-7

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13771-72-7 Usage

Description

(5-Bromo-benzo[b]thiophen-2-yl)-methanol is a pharmacologically active benzo[b]thiophene derivative, characterized by its unique chemical structure that includes a bromine atom at the 5-position and a hydroxyl group attached to the 2-position of the benzo[b]thiophene ring. (5-Bromo-benzo[b]thiophen-2-yl)-methanol exhibits significant potential in various pharmaceutical applications due to its bioactivity and structural properties.

Uses

Used in Pharmaceutical Industry:
(5-Bromo-benzo[b]thiophen-2-yl)-methanol is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of new drugs with potential therapeutic benefits in treating different medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5-Bromo-benzo[b]thiophen-2-yl)-methanol serves as a valuable building block for the design and synthesis of novel bioactive molecules. Its structural features enable researchers to explore new chemical space and develop innovative therapeutic agents with improved pharmacological properties.
Used in Drug Discovery and Development:
(5-Bromo-benzo[b]thiophen-2-yl)-methanol is utilized as a starting material in drug discovery and development processes. Its pharmacological activity and chemical versatility make it an attractive candidate for the creation of new drug candidates targeting a wide range of diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 13771-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13771-72:
(7*1)+(6*3)+(5*7)+(4*7)+(3*1)+(2*7)+(1*2)=107
107 % 10 = 7
So 13771-72-7 is a valid CAS Registry Number.

13771-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Bromo-benzo[b]thiophen-2-yl)-methanol

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-5-brom-benzo<b>thiophen

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:13771-72-7 SDS

13771-72-7Relevant articles and documents

Benzothiophene-flanked diketopyrrolopyrrole polymers: Impact of isomeric frameworks on carrier mobilities

Huang, Jianyao,Liu, Xiaotong,Gao, Dong,Wei, Congyuan,Zhang, Weifeng,Yu, Gui

, p. 83448 - 83455 (2016/10/22)

Exploring new building blocks for solution-processable polymeric semiconductors has attracted much attention. We herein develop two isomeric benzothiophene-flanked diketopyrrolopyrrole polymers with different linkage positions and further systematically study the electronic structures, optical properties, and field-effect characteristics. Both polymers exhibit typical p-type transport characteristics with the highest mobility being up to 0.80 cm2 V-1 s-1. Our results suggest that the isomeric backbones for conjugated polymers greatly affect charge transport properties.

CYCLOALKYL LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1

-

Page/Page column 63, (2008/06/13)

The present invention provides compounds of formula I that are useful as potent and selective inhibitors of 11-beta hydroxysteroid dehydrogenase 1. The present invention further provides a pharmaceutical composition which comprises a compound of Formula I, or a pharmaceutical salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient. In addition, the present invention provides compositions comprising compounds of formula I for the treatment of metabolic syndrome, diabetes, hyperglycemia, obesity, hypertension, hyperlipidemia, other symptoms associated with hyperglycemia, and related disorders. Formula (I) wherein, R0 is (II), or (III) G1 is methylene or ethylene; L is a divalent linking group selected from -(C1-C4) alkylene-, -S-, -CH(OH)-, or -O-; A is methylene, -S-, -O-, or -NH-; and the other substituents are as defined in the claims.

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