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31704-80-0

31704-80-0

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31704-80-0 Usage

Chemical Properties

3-(5-Methyl-2-furyl)butanal has vegetable, fruity, fatty undertones.

Uses

3-(5-Methyl-2-furyl)butyraldehyde can be used as antiviral agents.

Taste threshold values

Taste characteristics at 10 ppm: green, fruity with fatty nuances.

Check Digit Verification of cas no

The CAS Registry Mumber 31704-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31704-80:
(7*3)+(6*1)+(5*7)+(4*0)+(3*4)+(2*8)+(1*0)=90
90 % 10 = 0
So 31704-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-7(5-6-10)9-4-3-8(2)11-9/h3-4,6-7H,5H2,1-2H3/t7-/m1/s1

31704-80-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (B22671)  3-(5-Methyl-2-furyl)butyraldehyde, 99%   

  • 31704-80-0

  • 5g

  • 350.0CNY

  • Detail

  • Alfa Aesar

  • (B22671)  3-(5-Methyl-2-furyl)butyraldehyde, 99%   

  • 31704-80-0

  • 25g

  • 773.0CNY

  • Detail

  • Alfa Aesar

  • (B22671)  3-(5-Methyl-2-furyl)butyraldehyde, 99%   

  • 31704-80-0

  • 100g

  • 2403.0CNY

  • Detail

31704-80-0SDS

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 3-(5-methylfuran-2-yl)butanal

1.2 Other means of identification

Product number -
Other names 2-Furanpropanal,b,5-dimethyl

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:31704-80-0 SDS

31704-80-0Downstream Products

31704-80-0Relevant articles and documents

THE EFFECT OF SIDE CHAIN SUBSTITUENTS ON THE INTRAMOLECULAR DIELS-ALDER REACTION OF THE FURAN DIENE: THE SYNTHESIS OF (+/-)-1,4-EPOXYCADINANE

Rogers, Christine,Keay, Brian A.

, p. 1349 - 1352 (1989)

The effect of side chain substituents on the Intramolecular Diels-Alder reaction of the Furan diene (IMDAF) is reported in which the side chain connecting the furan diene to the dienophile contain four carbon atoms.The synthesis of 1,4-epoxycadinane utili

2,9-DIOXABICYCLONONAN-DARSTELLUNG, MASSENSPEKTROSKOPIE UND UMLAGERUNG EINES NEUEN HETEROCYCLISCHEN SYSTEMS

Francke, Wittko,Reith, Wolfgang

, p. 2029 - 2032 (2007/10/02)

Nine different methyl-substituted compounds of a new acetal system 5 are synthesized from 4-(5-methyl-2-furyl)alkanoles 1 and are rearranged to ketones 6; mass spectroscopic fragmentation patterns are described.

THE BF3-CATALYSED REACTION BETWEEN 2-METHYLFURAN AND SOME α,β-UNSATURATED CARBONYL COMPOUNDS.

ApSimon, J.,Srinivasan, V. Seenu,L'Abbe, M. R.,Seguin, R.

, p. 1079 - 1081 (2007/10/02)

The reaction of 2-methylfuran with some αβ unsaturated compounds in the presence of BF3-etherate is described as well as studies of the cleavage of the furan ring of the products.Only 1,4-addition to the conjugated carbonyl system is observed even in the

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