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Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]is a complex chemical compound characterized by its unique molecular structure. It features a methyl group, a fluorophenyl group, and a benzo[b]thien-2-ylMethyl group, all connected to a central carbon atom. Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]likely has pharmaceutical or industrial applications, potentially serving as a molecular scaffold for drug development or as a building block for organic synthesis. The presence of the fluorophenyl and benzo[b]thien-2-ylMethyl groups suggests that it may possess specific chemical and biological properties. Further research and testing are required to determine its exact characteristics and potential uses.

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  • 1034305-23-1 Structure
  • Basic information

    1. Product Name: Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]-
    2. Synonyms: Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]-;Methyl 1-C-[3-(benzo[b]thien-2-ylmethyl)-4-fluorophenyl]-alpha-D-glucopyranoside;(2S,3R,4S,5S,6R)-2-(3-(benzo[b]thiophen-2-ylMethyl)-4-fluorophenyl)-6-(hydroxyMethyl)-2-Methoxytetrahydro-2H-pyran-3,4,5-triol;Ipragliflozin impurity A (C7);Methyl 1-C-[3-(1-benzothien-2-ylmethyl)-4-fluorophenyl]-alpha-glucopyranoside;Methyl 1-C-[3-(benzo[b]thien-2-ylmethyl)-4-fluorophenyl]-α-D-glucopyranoside
    3. CAS NO:1034305-23-1
    4. Molecular Formula: C22H23FO6S
    5. Molecular Weight: 434.4778232
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1034305-23-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]-(1034305-23-1)
    11. EPA Substance Registry System: Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]-(1034305-23-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1034305-23-1(Hazardous Substances Data)

1034305-23-1 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]is used as a molecular scaffold for drug development due to its unique molecular structure and the presence of fluorophenyl and benzo[b]thien-2-ylMethyl groups. These groups may confer specific chemical and biological properties that can be exploited in the design of new pharmaceutical agents.
Used in Organic Synthesis:
Methyl 1-C-[3-(benzo[b]thien-2-ylMethyl)-4-fluorophenyl]is used as a building block in organic synthesis. Its complex molecular structure and functional groups make it a valuable component in the synthesis of various organic compounds, potentially leading to the development of new materials and chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 1034305-23-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,3,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1034305-23:
(9*1)+(8*0)+(7*3)+(6*4)+(5*3)+(4*0)+(3*5)+(2*2)+(1*3)=91
91 % 10 = 1
So 1034305-23-1 is a valid CAS Registry Number.

1034305-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 1-C-[3-(benzo[b]thien-2-ylmethyl)-4-fluorophenyl]-α-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names Methyl 1-C-[3-(benzo[b]thien-2-ylmethyl)-4-fluorophenyl]-alpha-D-glucopyranoside

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:1034305-23-1 SDS

1034305-23-1Relevant articles and documents

Preparing methods of ipragliflozin intermediates

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Page/Page column 8-11, (2018/04/01)

The invention discloses preparing methods of ipragliflozin intermediates. The methods includes preparing methods for 2-(3-benzo[B]thien-2-ylmethyl-4-fluorophenyl)-3,4,5-tris(trimethylsiloxy)-6-trimethylsiloxymethyl-tetrahydro-pyran-2-ol (a compound 3) and (1S)-2,3,4,6-tetraacetoxy-1,5-anhydro-1-[3-(1-benzothiophen-2-yl-methyl)-4-fluorophenyl]-D-glucitol (a compound 6). Under the premise of controlling the temperature of a reaction solution to be not higher than -60 DEG C, n-butyllithium should be added dropwise as soon as possible, and the higher the adding speed of the n-butyllithium is, theless F-ortho-position substituted side products of the compound 3 are, thus ensuring purity of the compound 3 and directly influencing the yield of the compound 6 finally prepared. Through scale-up, the methods are free of scale-up effects, and are suitable for industrial production.

C-glycoside derivative method for manufacturing

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Paragraph 0024; 0025, (2017/02/23)

The subject of this invention is to provide a high efficiency and industrial conditions in order to facilitate manufacturing C-glycoside derivative technology. Use of the aryl magnesium acid salt (aryl magnesate) the coupling reaction, thereby can prevent the ultra-low temperature reaction, and at the same time, can be short time and high-yield manufacturing C-glycoside derivative.

METHOD FOR PRODUCING C-GLYCOSIDE DERIVATIVE AND SYNTHETIC INTERMEDIATE THEREOF

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Page/Page column 14, (2009/10/06)

The present invention provides a method for producing a C-glycoside derivative, which can produce the C-glycoside derivative at a high yield and at a low cost, which conforms to environmental protection, and which is applicable industrially. The C-glycoside derivative is useful for treating and preventing diabetes such as insulin-dependent diabetes (type 1 diabetes), non-insulin-dependent diabetes (type 2 diabetes) and the like and various diabetes-related diseases including insulin-resistant diseases and obesity.

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