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2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 42031-02-7 Structure
  • Basic information

    1. Product Name: 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane
    2. Synonyms: 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane
    3. CAS NO:42031-02-7
    4. Molecular Formula:
    5. Molecular Weight: 400.472
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 42031-02-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane(42031-02-7)
    11. EPA Substance Registry System: 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane(42031-02-7)
  • 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: 42031-02-7(Hazardous Substances Data)

42031-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42031-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,3 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42031-02:
(7*4)+(6*2)+(5*0)+(4*3)+(3*1)+(2*0)+(1*2)=57
57 % 10 = 7
So 42031-02-7 is a valid CAS Registry Number.

42031-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis-(p-ethoxycarbonylmethoxyphenyl)propane

1.2 Other means of identification

Product number -
Other names (4-[1-(4-ethoxycarbonylmethoxy-phenyl)-1-methyl-ethyl]-phenoxy)-acetic acid ethyl ester

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:42031-02-7 SDS

42031-02-7Relevant articles and documents

Ultrasound-assisted synthesis of 2,5-dimethyl-N-substituted pyrroles catalyzed by uranyl nitrate hexahydrate

Satyanarayana,Sivakumar

scheme or table, p. 917 - 922 (2012/03/08)

An efficient synthesis of different novel 2,5-dimethyl-N-substituted pyrrole derivatives by the Paal-Knorr condensation has been accomplished using uranyl nitrate hexahydrate as catalyst under soft conditions and ultrasonic irradiation. The synthesized compounds were confirmed through spectral characterization using IR, 1H NMR, 13C NMR and mass spectra.

Dihydroxy aromatic compounds and methods for preparation

-

Page/Page column 16-17, (2010/11/25)

A dihydroxy aromatic compound having a Formula (I), wherein R1 is a C6–C60 aromatic divalent functionality, R2 at each occurrence, can be the same or different and is independently at each occurrence selected from the group consisting of a cyano functionality, a nitro functionality, a halogen, an aliphatic functionality having 1 to 10 carbons, a cycloaliphatic functionality having 3 to 10 carbons and an aromatic functionality having 6 to 10 carbons, and “n” is an integer having a value of 0 to 4.

Tryptase inhibitors

-

, (2008/06/13)

The invention relates to novel inhibitors of human tryptase which are used in the pharmaceutical industry for the production of medicaments.

Molecular recognition of β-ribofuranosides by synthetic polypyridine-macrocyclic receptors

Inouye, Masahiko,Miyake, Toshiyuki,Furusyo, Masaru,Nakazumi, Hiroyuki

, p. 12416 - 12425 (2007/10/03)

Artificial ribofuranoside receptors were designed and synthesized. The design of the polypyridine-macrocyclic receptors was based on the multipoint hydrogen bond complementarity between the receptors and methyl β-D-ribofuranoside. The binding affinity of the receptors for the ribofuranoside in CDCl3 was very high (up to K(a) = 5.2 x 103 M-1), so that even native ribose was extracted by them into such nonpolar solvents. Selective extraction of ribose by the receptors was observed: the extractabilities, or affinities to the receptors of various pentoses and hexoses decreased in the following order: ribose > deoxyribose ? lyxose ? xylose > fructose > arabinose > glucose ? mannose ? galactose. The selectivity is governed by the OH direction and the whole size of the sugars as well as their shapes. Furthermore, fluorescence emission of the receptors was largely enhanced in the presence of methyl β-D-ribofuranoside or ribose, and the degree for the fluorescence enhancement by the addition of various sugars was almost compatible with that of the extractabilities. The polypyridine-macrocycles represent rationally designed multifunctional artificial receptors for ribofuranosides.

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