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57818-37-8

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57818-37-8 Usage

Uses

3-Methyl-5-pentyl-2-furanundecanoic Acid is also known as F5 furan fatty acid. Furan fatty acids are generated in large amounts in algae and fish, but they are also produced by plants and microorganisms. Furan fatty acids are known to exhibit radical-scavenging ability and anti-inflammatory properties.

Check Digit Verification of cas no

The CAS Registry Mumber 57818-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,1 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57818-37:
(7*5)+(6*7)+(5*8)+(4*1)+(3*8)+(2*3)+(1*7)=158
158 % 10 = 8
So 57818-37-8 is a valid CAS Registry Number.

57818-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-(3-methyl-5-pentylfuran-2-yl)undecanoic acid

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:57818-37-8 SDS

57818-37-8Downstream Products

57818-37-8Relevant articles and documents

Optimised total syntheses of the F-furan fatty acids F5 and F6 and some deuterated derivatives Dedicated, with the greatest respect, to the memory of Professor Alan R. Katritzky

Knight, David W.,Smith, Andrew W.T.

, p. 7436 - 7444 (2015/08/24)

Optimised syntheses of F5- and F6-furan fatty acids 2 and 3 are described in full. Key steps include furan formation from a single 3-alkyne-1,2-diol 6 using 5-endo-dig cyclisations triggered by silver(I) nitrate or iodine. Introducti

Total synthesis of the naturally occurring furanoid fatty acid, F5

Marson, Charles M.,Harper, Steven

, p. 333 - 334 (2007/10/03)

The furanoid fatty acid F5 has been synthesized using a mercury(II) catalyzed isomerization of 2-(1,2-oxiranylcyclododecyl)-3-nonyn-2-ol.

Sequential Pd(0)-catalyzed reactions for the construction of multiple substituted furans. A short synthesis of the F5 furan fatty acid

Bach, Thorsten,Krueger, Lars

, p. 1729 - 1732 (2007/10/03)

4,5-Dibromofurfural (1) undergoes a regioselective Pd(0)-catalyzed C-C bond forming reaction at its C-5 position to yield corresponding furans 3. The second bromine substituent in C-4 position can be substituted by a methyl group in a subsequent Pd(0)-catalyzed cross coupling reaction. The furan fatty acid 12 and its benzyl ester 13 were prepared in a short synthetic sequence using this method.

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