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2-(acetyloxy)cyclopentyl 4-nitrobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37844-68-1

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37844-68-1 Usage

Class

Esters

Composition

Cyclopentyl group attached to a 4-nitrobenzoate group, with an acetyloxy substitution on the cyclopentyl group

Usage

Chemical research and synthesis (reagent or intermediate), pharmaceutical industry, building block for new drug development

Significance

Unique structure and properties, of interest to researchers in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 37844-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37844-68:
(7*3)+(6*7)+(5*8)+(4*4)+(3*4)+(2*6)+(1*8)=151
151 % 10 = 1
So 37844-68-1 is a valid CAS Registry Number.

37844-68-1SDS

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-acetyloxycyclopentyl) 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names cis-1-acetoxycyclopentan-2-ol p-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:37844-68-1 SDS

37844-68-1Downstream Products

37844-68-1Relevant academic research and scientific papers

The Use of Bismuth(III) Acetate in 'Wet' and 'Dry' Prevost Reactions

Trainor, Robert W.,Deacon, Glen B.,Jackson, W. Roy,Giunta, Nunzio

, p. 1265 - 1280 (2007/10/02)

cis-Diol and trans-diol derivatives can be prepared from alkenes by reaction with iodine and bismuth(III) acetate in 'wet' and 'dry' acetic acid, respectively.Reactions using lesser amounts of bismuth(III) acetate under 'dry' conditions give iodo acetates and under 'wet' conditions a mixture of iodohydrins and iodo ethers.Comparison of these reactions with those promoted by silver, copper, mercury and thallium salts is included.

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