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114012-05-4

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114012-05-4 Usage

Appearance

Pale yellow to brown solid

Odor

Slightly floral

Usage

Antioxidant in rubber, petroleum products, and lubricants

Purpose

To prevent degradation from heat and oxygen exposure

Potential use

In pharmaceuticals and as a precursor to other organic compounds

Safety precautions

Causes irritation to skin, eyes, and respiratory system; toxic to aquatic organisms

Check Digit Verification of cas no

The CAS Registry Mumber 114012-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114012-05:
(8*1)+(7*1)+(6*4)+(5*0)+(4*1)+(3*2)+(2*0)+(1*5)=54
54 % 10 = 4
So 114012-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO2/c15-13-8-4-5-9-14(13)17-11-10-16-12-6-2-1-3-7-12/h1-9H,10-11,15H2

114012-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-phenoxyethoxy)aniline

1.2 Other means of identification

Product number -
Other names -

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:114012-05-4 SDS

114012-05-4Relevant articles and documents

SYNTHESIS OF BAPTA-AM ANALOGUES CAPABLE OF ENHANCING THE VASCULAR PRODUCTION OF PROSTACYCLIN

Heilporn, S.,Broeders, F.,Daloze, D.,Braekman, J. C.,Boeynaems, J. M.

, p. 309 - 320 (2007/10/02)

About 30 analogues of BAPTA-AM, a potential antithrombotic agent, have been synthesized and tested for their effect on the production of prostacyclin.None of them was found to be a better enhancher of the production of prostacyclin by aortic endothelial cells than BAPTA-AM itself.The enhancing effect can be produced by compounds unable to chelate Ca2+, thus confirming that it is not related to their buffering capacity for free Ca2+.

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