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Tridecanoic acid, 13-oxo-, methyl ester is a chemical compound with the molecular formula C14H26O3. It is an ester derivative of 13-oxotridecanoic acid, where the carboxyl group is replaced by a methyl group. This organic compound is characterized by a long aliphatic chain with a carbonyl group at the 13th position, indicating the presence of a ketone functional group. It is a colorless liquid with a specific odor and is insoluble in water but soluble in organic solvents. Tridecanoic acid, 13-oxo-, methyl ester has potential applications in the synthesis of various chemicals, pharmaceuticals, and as a precursor in the production of fragrances and flavorings. Due to its specific structure, it may also be used in research and development for understanding the properties and reactions of similar compounds.

1608-77-1

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1608-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1608-77:
(6*1)+(5*6)+(4*0)+(3*8)+(2*7)+(1*7)=81
81 % 10 = 1
So 1608-77-1 is a valid CAS Registry Number.

1608-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 12-formyldodecanoate

1.2 Other means of identification

Product number -
Other names Methyl 13-Oxotridecanoate

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:1608-77-1 SDS

1608-77-1Relevant academic research and scientific papers

Fe-catalyzed one-pot oxidative cleavage of unsaturated fatty acids into aldehydes with hydrogen peroxide and sodium periodate

Spannring, Peter,Yazerski, Vital,Bruijnincx, Pieter C. A.,Weckhuysen, Bert M.,Klein Gebbink, Robertus J. M.

, p. 15012 - 15018 (2013/11/06)

A one-pot method has been developed for the oxidative cleavage of internal alkenes into aldehydes by using 0.5mol % of the nonheme iron complex [Fe(OTf)2(mix-bpbp)] (bpbp=N,N'-bis(2-picolyl)-2,2'-bipyrrolidine) as catalyst and 1.5equivalents of hydrogen peroxide and 1equivalent of sodium periodate as oxidants. A mixture of diastereomers of the chiral bpbp ligand can be used, thereby omitting the need for resolution of its optically active components. The cleavage reaction can be performed in one pot within 20h and under ambient conditions. Addition of water after the epoxidation, acidification and subsequent pH neutralization are crucial to perform the epoxidation, hydrolysis, and subsequent diol cleavage in one pot. High aldehyde yields can be obtained for the cleavage of internal aliphatic double bonds with cis and trans configuration (86-98 %) and unsaturated fatty acids and esters (69-96 %). Good aldehyde yields are obtained in reactions of trisubstituted and terminal alkenes (62-63 %). The products can be easily isolated by a simple extraction step with an organic solvent. The presented protocol involves a lower catalyst loading than conventional methods based on Ru or Os. Also, hydrogen peroxide can be used as the oxidant in this case, which is often disproportionated by second- and third-row metals. By using only mild oxidants, overoxidation of the aldehyde to the carboxylic acid is prevented. Copyright

Safe use of a toxic compound: Heterogeneous OsO4 catalysis in a nanobrush polymer microreactor

Basavaraju,Sharma, Siddharth,Maurya, Ram Awatar,Kim, Dong-Pyo

, p. 6735 - 6738 (2013/07/26)

Putting osmium in its place: The immobilization of hazardous OsO 4 on polymer nanobrushes in a microreactor is a safe, effective, and green concept. The method allows reactions to be performed in a time- and chemical-saving manner, with little environmental impact, as compared to spill-over bulk processes. Copyright

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