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2-AMino-1-(Oxan-4-yl)ethan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

911060-79-2

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911060-79-2 Usage

Derivative of

Ethanol

Functional Groups

Amino Group (NH2)
Oxan-4-yl Group (C4H7O)

Class

Alcohols and Amines

Utility

Organic Synthesis
Pharmaceutical Research

Potential Applications

Drug Development
Bioactive Compound Synthesis

Versatility

Building Block for Organic Compound Synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 911060-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,0,6 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 911060-79:
(8*9)+(7*1)+(6*1)+(5*0)+(4*6)+(3*0)+(2*7)+(1*9)=132
132 % 10 = 2
So 911060-79-2 is a valid CAS Registry Number.

911060-79-2SDS

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-amino-1-(oxan-4-yl)ethanol

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:911060-79-2 SDS

911060-79-2Upstream product

911060-79-2Downstream Products

911060-79-2Relevant academic research and scientific papers

Synthesis of tri- and tetrasubstituted imidazoles

Paone, Daniel V.,Shaw, Anthony W.

scheme or table, p. 6155 - 6159 (2009/04/05)

A reliable sequence that allows for regiospecific incorporation of four alkyl substituents on an imidazole ring has been developed. This procedure involves the addition of a substituted amino alcohol to a thioamide and subsequent oxidation with PDC. Unlike many imidazole syntheses, acid-sensitive functionality is tolerated given the mild conditions.

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