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79324-95-1

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79324-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79324-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79324-95:
(7*7)+(6*9)+(5*3)+(4*2)+(3*4)+(2*9)+(1*5)=161
161 % 10 = 1
So 79324-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4/c9-5-7-2-1-6(12-7)3-4-8(10)11/h1-4,9H,5H2/b4-3+

79324-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name {5-[(E)-2-Nitrovinyl]-2-furyl}methanol

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:79324-95-1 SDS

79324-95-1Downstream Products

79324-95-1Relevant articles and documents

Facile synthesis of 5-hydroxymethylfurfural: A sustainable raw material for the synthesis of key intermediates toward 21,23-dioxaporphyrins

Rajmohan, Rajamani,Gayathri, Subramaniyan,Vairaprakash, Pothiappan

, p. 100401 - 100407 (2015)

In a simple and conceptually designed method for the dehydration of fructose on a solid support, 5-hydroxymethylfurfural (HMF) was synthesized in more than 95% isolated yield from fructose under very mild conditions at room temperature. The loading of fructose on the solid support reduced the intermolecular interactions between fructose/intermediates, diminished the formation of polymeric material (humin) and increased the selectivity towards HMF formation. The synthesized HMF was readily converted into key intermediates toward the simpler synthesis of 21,23-dioxaporphyrins.

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