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16428-47-0

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16428-47-0 Usage

General Description

2-AMINO-1-(4-NITROPHENYL)ETHANOL, also known as 4-Nitrophenethanol, is a chemical compound with the molecular formula C8H9NO3. It is a pale yellow solid that is commonly used as an intermediate in the manufacture of pharmaceuticals and other organic compounds. 4-Nitrophenethanol is also used as a reagent in organic synthesis, particularly in the formation of esters and ethers. It is known to have antibacterial properties and has been used in the development of antimicrobial agents. Additionally, it has been studied for its potential application in the treatment of cancer due to its ability to inhibit certain enzymes involved in cancer cell growth. However, 4-Nitrophenethanol is considered toxic and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 16428-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16428-47:
(7*1)+(6*6)+(5*4)+(4*2)+(3*8)+(2*4)+(1*7)=110
110 % 10 = 0
So 16428-47-0 is a valid CAS Registry Number.

16428-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(4-nitrophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(4-nitrophenyl)ethanol HCl

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:16428-47-0 SDS

16428-47-0Relevant articles and documents

Lewis acid mediated intramolecular C-O bond formation of alkanol-epoxide leading to substituted morpholine and 1,4-oxazepane derivatives: Total synthesis of (±)-Viloxazine

Ghosh, Priya,Deka, Manash J.,Saikia, Anil K.

, p. 690 - 698 (2016/01/15)

Substituted morpholines have been efficiently synthesised in good yields from nitrogen tethered alkanol-epoxide mediated by boron trifluoride etherate. The methodology has been used for the total synthesis of (±)-viloxazine.

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