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N-{[2-acetyl-7-(pentyloxy)-1-benzofuran-4-yl]sulfonyl}glycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105668-57-3 Structure
  • Basic information

    1. Product Name: N-{[2-acetyl-7-(pentyloxy)-1-benzofuran-4-yl]sulfonyl}glycine
    2. Synonyms: Glycine, N-[[2-acetyl-7-(pentyloxy)-4-benzofuranyl]sulfonyl]-
    3. CAS NO:105668-57-3
    4. Molecular Formula: C17H21NO7S
    5. Molecular Weight: 383.4161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105668-57-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 587.6°C at 760 mmHg
    3. Flash Point: 309.2°C
    4. Appearance: N/A
    5. Density: 1.323g/cm3
    6. Vapor Pressure: 1.19E-14mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-{[2-acetyl-7-(pentyloxy)-1-benzofuran-4-yl]sulfonyl}glycine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-{[2-acetyl-7-(pentyloxy)-1-benzofuran-4-yl]sulfonyl}glycine(105668-57-3)
    12. EPA Substance Registry System: N-{[2-acetyl-7-(pentyloxy)-1-benzofuran-4-yl]sulfonyl}glycine(105668-57-3)
  • 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: 105668-57-3(Hazardous Substances Data)

105668-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105668-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,6 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105668-57:
(8*1)+(7*0)+(6*5)+(5*6)+(4*6)+(3*8)+(2*5)+(1*7)=133
133 % 10 = 3
So 105668-57-3 is a valid CAS Registry Number.

105668-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-acetyl-7-pentoxy-1-benzofuran-4-yl)sulfonylamino]acetic acid

1.2 Other means of identification

Product number -
Other names 2-acetyl-4-carboxymethylsulfamoyl-7-pentyloxybenzo<b>furan

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:105668-57-3 SDS

105668-57-3Downstream Products

105668-57-3Relevant articles and documents

Benzofuran derivatives useful in treating diabetic complications

-

, (2008/06/13)

A benzofuran derivative having the general formula (I): STR1 wherein R1 is hydrogen atom, a benzyl group, unsubstituted or substituted with a halogen atom or an alkyloxy group, or an alkyl group having 1 to 3 carbon atoms, R2 is hydrogen atom or an alkyl group having 1 to 3 carbon atoms, R3 is acetyl group, ethyl group, carboxyl group or 4-methyl-2,5-dioxoimidazolidine-4-yl group, R4 is hydrogen atom, hydroxyl group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 9 carbon atoms, carboxymethoxy group, nitro group, acetoamino group, a benzylozy group unsubstituted or substituted with a halogen atom, nitro group or an alkyloxy group or a group having the formula: --OR6, wherein R6 is an alkenyl group having 2 to 4 carbon atoms or an alkyl group having 2 to 3 carbon atoms having a halogen atom, cyano group or oxo group, R5 is hydrogen atom or methylenedioxy group together with R4 group, n is 1 or 2, and the unsubstituted or substituted N-carboxymethylsulfamoyl group, R4 and R5 are attached at 3-position, 4-position, 5-position, 6-position or 7-position of the benzofuran ring, or a nontoxic salt thereof, process for preparing the same and a pharmaceutical composition containing the same. The compounds of the present invention have powerful aldose reductase inhibiting activity, platelet aggregation inhibiting activity and arachidonic acid metabolism inhibiting activity and are useful for a remedy for treatment of diabetic complications.

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