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6-Octenoic acid, 5-(benzoyloxy)-7-methyl, ethyl ester, (S)- is a complex organic compound with the chemical formula C18H24O4. It is a chiral molecule, with the (S)-configuration indicating the specific arrangement of atoms in the molecule. 6-Octenoic acid, 5-(benzoyloxy)-7-methyl-, ethyl ester, (S)- is characterized by a long hydrocarbon chain with a double bond at the 6th position, a methyl group at the 7th position, and a benzoyloxy group at the 5th position. The ethyl ester group is attached to the carboxylic acid end, indicating that it is an ester derivative of the parent 6-octen-5-ynoic acid. 6-Octenoic acid, 5-(benzoyloxy)-7-methyl-, ethyl ester, (S)- is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and functional groups.

137522-15-7

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137522-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137522-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,5,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137522-15:
(8*1)+(7*3)+(6*7)+(5*5)+(4*2)+(3*2)+(2*1)+(1*5)=117
117 % 10 = 7
So 137522-15-7 is a valid CAS Registry Number.

137522-15-7SDS

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 (S)-ethyl 5-benzoyloxy-7,7-dimethylhept-6-enoate

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

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More Details:137522-15-7 SDS

137522-15-7Relevant academic research and scientific papers

Use of the Two Enantiometers of 7,7-Dimethylbicyclohept-2-en-6-one to form Complementary Optically Active Synthons in a Convergent Synthesis of Leukotriene-B4

Cotterill, Ian C.,Jaouhari, Rabih,Dorman, Gyoergy,Roberts, Stanley M.,Scheinmann, Feodor,Wakefield, Basil J.

, p. 2505 - 2512 (2007/10/02)

The acetate (+/-)-4 was resolved by an enantioselective hydrolysis catalysed by porcine pancreatic lipase.The resultant alcohol (-)-3 and the optically active ester (+)-4 were converted into the ketones (+)-2 and (-)-2 respectively.The ketone (+)-2 was el

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