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Benzenemethanol, 4-amino-a-(aminomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15015-45-9

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15015-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15015-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15015-45:
(7*1)+(6*5)+(5*0)+(4*1)+(3*5)+(2*4)+(1*5)=69
69 % 10 = 9
So 15015-45-9 is a valid CAS Registry Number.

15015-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<4-Amino-phenyl>-2-hydroxy-aethylamin

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(4-amino-phenyl)-aethan-1-ol

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:15015-45-9 SDS

15015-45-9Relevant academic research and scientific papers

Synthesis and cytotoxicity of 1-phenylethanolamine carboxamide derivatives: Effects on the cell cycle

Babu, Balaji,Forrest, Lori,Weisbruch, Paul,Chavda, Sameer,Pati, Hari,Lee, Moses

, p. 1141 - 1152 (2011/10/03)

Seven novel analogues of 1-phenylethanolamine carboxamide derivatives, 3a-3g, related to carboxamides isolated from Isodon excisus were synthesized and evaluated for their cytotoxic and apoptosis-induction properties against murine B16 and leukemia L1210 cell lines. Compounds containing no substitution at the 4′-position (3a-3d) or containing a 4′-amino (3e-3g) group were investigated. Generally, the amino-containing compounds were slightly more active than their unsubstituted congeners. Also, the indole-containing compounds 3c and 3f gave the strongest cytotoxic activity (IC50 = 25-87 μM) against the growth of L1210 and B16 cancer cells. Compound 3f was subjected to flow cytometry studies and it was found to induce L1210 cells grown in culture to undergo apoptosis.

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