71317-67-4 Usage
Description
(3Z,5Z)-15-Chloro-3,5-pentadecadiene is a chlorinated diene chemical compound with the molecular formula C15H25Cl. It is characterized by the presence of two double bonds and a chlorine atom. This colorless liquid at room temperature is mainly utilized in organic synthesis and chemical research.
Uses
Used in Chemical Research:
(3Z,5Z)-15-Chloro-3,5-pentadecadiene is used as a research compound for studying the reactivity of dienes and for developing new organic reactions. Its unique structure and properties make it a valuable tool in advancing the field of chemical research and development.
Used in Organic Synthesis:
(3Z,5Z)-15-Chloro-3,5-pentadecadiene is used as a precursor in organic synthesis for the synthesis of other organic compounds. Its versatility in chemical reactions contributes to the creation of a wide range of chemical products, making it an important component in the field of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 71317-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,1 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71317-67:
(7*7)+(6*1)+(5*3)+(4*1)+(3*7)+(2*6)+(1*7)=114
114 % 10 = 4
So 71317-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H27Cl/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h3-6H,2,7-15H2,1H3/b4-3-,6-5-
71317-67-4Relevant articles and documents
Synthesis of (Z,Z)-11,13-Hexadecadienal, a Principal Component of Navel Orangeworm (Pamyelois transitella) Pheromone
Bishop, Clyde E.,Morrow, Gary W.
, p. 657 - 660 (1983)
This report outlines a commercial synthetic process for (Z,Z)-11,13-hexadecadienal (navel orangeworm pheromone).The synthetic scheme which is employed introduces the stereochemically labile conjugated diene moiety at a late stage in the synthesis, thereby avoiding complications during the purification of intermediates.In addition, the aldehyde function is generated through a Grignard reaction sequence, obviating the generally accepted techniques which are usually unsuitable for commercial preparations.We have also observed the first reported selective inclusion by urea of a conjugated (Z,Z)-diene as a means of mild purification of labile dienic pheromone intermediates.
