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36144-39-5

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36144-39-5 Usage

Type of compound

Nitrobenzoate ester derivative of ethynylcyclohexane

Common use

Organic and pharmaceutical synthesis

Potential applications

Medicinal chemistry, development of new drugs and pharmaceutical products

Chemical structure

Suggests possible pharmacological properties

Research interest

Drug discovery field

Properties and reactivity

Valuable building block for synthesis of various organic compounds in the laboratory

Check Digit Verification of cas no

The CAS Registry Mumber 36144-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,4 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36144-39:
(7*3)+(6*6)+(5*1)+(4*4)+(3*4)+(2*3)+(1*9)=105
105 % 10 = 5
So 36144-39-5 is a valid CAS Registry Number.

36144-39-5SDS

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 (1-ethynylcyclohexyl) 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 1-ethynylcyclohexyl 4-nitrobenzoate

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:36144-39-5 SDS

36144-39-5Relevant articles and documents

Mild and selective sodium azide mediated cleavage of p-nitrobenzoic esters.

Gomez-Vidal,Forrester,Silverman

, p. 2477 - 2479 (2007/10/03)

[reaction: see text] A mild and selective cleavage of p-nitrobenzoic esters by sodium azide in methanol is reported. This new methodology is mild enough for use with acid- or base-sensitive compounds. No elimination byproducts are formed. Fmoc- and trifluoroacetyl-amino protecting groups, benzyl esters, and ethyl esters remain unaffected. Less reactive compounds are discussed in terms of steric factors, and yields are increased by altering the azide solvation.

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