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Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104354-26-9 Structure
  • Basic information

    1. Product Name: Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester
    2. Synonyms: Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester
    3. CAS NO:104354-26-9
    4. Molecular Formula: C12H14O4
    5. Molecular Weight: 222.23716
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104354-26-9.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester(104354-26-9)
    11. EPA Substance Registry System: Benzoic acid, 3-(oxiranylMethoxy)-, ethyl ester(104354-26-9)
  • 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: 104354-26-9(Hazardous Substances Data)

104354-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104354-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,5 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104354-26:
(8*1)+(7*0)+(6*4)+(5*3)+(4*5)+(3*4)+(2*2)+(1*6)=89
89 % 10 = 9
So 104354-26-9 is a valid CAS Registry Number.

104354-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(oxiran-2-ylmethoxy)benzoate

1.2 Other means of identification

Product number -
Other names ethyl 3-glycidyloxybenzoate

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:104354-26-9 SDS

104354-26-9Downstream Products

104354-26-9Relevant articles and documents

8-Substituted purine derivatives: a new class of lipid-lowering agents

Vanotti, E.,Bani, M.,Favara, D.,Gobetti, M.,Lombroso, M.,et al.

, p. 287 - 294 (2007/10/02)

A series of purine derivatives have been prepared and their in vivo abilities to lower plasma total cholesterol and triglyceride levels, and to elevate high density lipoprotein (HDL) cholesterol levels in hyperlipemic rats have been tested.Some compounds, among which 8-propylthio>adenosine 31, 8--2-oxopropylthio>adenosine 33 and 8--2-hydrazonecarboxamidepropylthio>adenosine 36 appear to be the most interesting, have been found to have both the desired profile of activity and no hepatotoxicity, when administered po at 50, 100 or 300 mg/kg.Compounds 31, 33 and 36, orally tested at the same doses in the 15-d test, lower triglyceride and VLDL/LDL (very low density lipoprotein / low density lipoprotein) cholesterol levels by 10-33percent and 13-46percent, respectively, and increase HDL-associated cholesterol levels by 10-32percent.These molecules have been chosen for further pharmacological and toxicological evaluations. adenosine / purine / cholesterol / triglyceride / hypolipemic agent

New 8-substituted nucleoside and purine derivatives, the process for the preparation thereof and the pharmaceutical compositions containing them

-

, (2008/06/13)

New 8-substituted nucleoside and purine derivatives of the general formula: STR1 wherein R represents an amino group or an hydroxy group possibly in the corresponding keto tautomeric form, R1 is hydrogen or an amino group, R2 is hydrogen or a β-D-ribofuranosyl radical wherein the primary hydroxy group and/or the two secondary hydroxy groups may be derivatized, R3 is an optionally substituted aryl or monocyclic heteroaryl radical and, X is --O-- or --S--. The new compounds have antihyperlipaemic activity.

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