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1-Benzothiophen-5-ylmethanol, a chemical compound with the molecular formula C9H8OS, is a white to off-white solid that is insoluble in water. It is a versatile and valuable chemical used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, dyes, and pigments. Its potential biological and pharmacological properties make it a promising building block in the development of new chemical entities.

20532-34-7

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20532-34-7 Usage

Uses

Used in Pharmaceutical Industry:
1-Benzothiophen-5-ylmethanol is used as a key intermediate in the synthesis of pharmaceuticals for its potential biological and pharmacological properties. It contributes to the development of new chemical entities with therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Benzothiophen-5-ylmethanol is utilized as a building block in the production of agrochemicals, such as pesticides and herbicides, due to its chemical properties and reactivity.
Used in Dye and Pigment Production:
1-Benzothiophen-5-ylmethanol is employed in the manufacturing of dyes and pigments, where its chemical structure and properties contribute to the color and stability of these products.
Used in Organic Compound Synthesis:
As a versatile chemical intermediate, 1-Benzothiophen-5-ylmethanol is used in the synthesis of various organic compounds, enabling the creation of new molecules with diverse applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 20532-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20532-34:
(7*2)+(6*0)+(5*5)+(4*3)+(3*2)+(2*3)+(1*4)=67
67 % 10 = 7
So 20532-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8OS/c10-6-7-1-2-9-8(5-7)3-4-11-9/h1-5,10H,6H2

20532-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BENZOTHIOPHEN-5-YLMETHANOL

1.2 Other means of identification

Product number -
Other names 5-Hydroxymethyl-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:20532-34-7 SDS

20532-34-7Relevant academic research and scientific papers

GAMMA-DIKETONES AS WNT/BETA -CATENIN SIGNALING PATHWAY ACTIVATORS

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Paragraph 1750; 1753, (2014/09/03)

The present disclosure provides γ-diketones or analogs thereof, that activate Wnt/β-catenin signaling and thus treat or prevent diseases related to signal transduction, such as osteoporosis and osteoarthropathy; osteogenesis imperfecta, bone defects, bone fractures, periodontal disease, otosclerosis, wound healing, craniofacial defects, oncolytic bone disease, traumatic brain injuries or spine injuries, brain atrophy/neurological disorders related to the differentiation and development of the central nervous system, including Parkinson's disease, strokes, ischemic cerebral disease, epilepsy, Alzheimer's disease, depression, bipolar disorder, schizophrenia; otic disorders like cochlear hair cell loss; eye diseases such as age related macular degeneration, diabetic macular edema or retinitis pigmentosa and diseases related to differentiation and growth of stem cell, such as hair loss, hematopoiesis related diseases and tissue regeneration related diseases.

NOVEL BENSOPHENONE DERIVATIVES OR SALTS THEREOF

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Page 130, (2010/02/07)

A benzophenone derivative represented by the following formula: whereinR1 represents, for example, an optionally substituted heterocyclic group, or a substituted phenyl group; Z represents, for example, an alkylene group; R2 represents, for example, a carboxyl group optionally protected with alkyl;R3 represents, for example, an optionally protected hydroxyl group; R4 represents, for example, an optionally substituted cycloalkyloxy group; and R5 represents, for example, a hydrogen atom, ???or a salt thereof has anti-arthritic activity, inhibits bone destruction caused by arthritis, and provides high safety and excellent pharmacokinetics and thus is useful as therapeutic agent for arthritis. These compounds have inhibitory effect on AP-1 activity and are useful as preventive or therapeutic agent for diseases in which excessive expression of AP-1 is involved.

A novel preparation of 2-naphthyl and 5-benzo[B]thienyl methanesulfonyl chlorides

Walker, Graham,Rana, Kishore K.

, p. 627 - 632 (2007/10/03)

Electron rich arylmethylsulfonyl chlorides can be prepared from arylmethyl bromides by phase transfer sulfonation and chlorination with PCl5.

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