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75631-81-1

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75631-81-1 Usage

General Description

The chemical compound "[2-(acetyloxy)-5-nitro-2,5-dihydrofuran-2-yl]methanediyl diacetate" is an ester formed from the combination of 2-(acetyloxy)-5-nitro-2,5-dihydrofuran-2-yl and methanediyl diacetate. It is a nitro compound with a diacetate functional group, and its molecular structure consists of a furan ring with nitro and acetyl groups attached. [2-(acetyloxy)-5-nitro-2,5-dihydrofuran-2-yl]methanediyl diacetate is commonly used in organic synthesis and pharmaceutical research due to its reactivity and potential pharmacological properties. It is important to handle and store this compound with appropriate safety measures, as it may pose hazards if mishandled.

Check Digit Verification of cas no

The CAS Registry Mumber 75631-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,3 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75631-81:
(7*7)+(6*5)+(5*6)+(4*3)+(3*1)+(2*8)+(1*1)=141
141 % 10 = 1
So 75631-81-1 is a valid CAS Registry Number.

75631-81-1SDS

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 cis-2-acetoxy-5-nitro-2,5-dihydro-2-furfural diacetate

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:75631-81-1 SDS

75631-81-1Relevant articles and documents

Nitronium Acetate Adducts of Furan Derivatives

Balina, Gisela,Kesler, Patricia,Petre, Janet,Pham, Dung,Vollmar, Arnulf

, p. 3811 - 3818 (2007/10/02)

An improved procedure for the isolation of the main addition products of the reaction between nitronium acetate and furfural diacetate or methyl 2-furoate is described.The kinetics of the deacetylation of the diastereomeric 1,4-adducts in buffer solutions revealed a substantial primary hydrogen isotope effect.Mild acid-induced alcoholysis transformed the adducts into 2,5-dialkoxy-2,5-dihydrofurans.The reaction chemistry of the furan adducts is compared with the solvolytic pathways reported for ipso nitronium acetate adducts formed from alkylbenzenes.

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