\n
$\"\"$ <\/p>\n<\/div>\n
In fact one synthesis uses the following as carbon sources:<\/p>\n
$\"\"$ <\/p>\n
cis (Z) jasmone , <\/span><\/strong><\/p>\n
cas no 488-10-8, 3-methyl-2-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-one<\/span><\/strong><\/p>\n
ref-(Can. J. Chem. 1978, Vol 56, p2301)<\/span><\/strong><\/p>\n
$\"\"$ <\/span><\/strong><\/p>\n
1\u00a0\u00a0\u00a0 W. Theilheimer. Synthetic Methods of Organic Chemistry. Volume 31, 1977, p. 352
\n2\u00a0\u00a0 Tetrahedron, 39 (24), p. 4127, 1983<\/span><\/strong><\/p>\n
<\/p>\n
\n
Thomas Koch, Katja Bandemer, Wilhelm Boland (1997). “Biosynthesis of cis-Jasmone: a pathway for the inactivation and the disposal of the plant stress hormone jasmonic acid to the gas phase?”.\u00a0Helvetica Chimica Acta<\/a><\/em>\u00a080<\/strong>\u00a0(3): 838\u2013850.doi<\/a>:10.1002\/hlca.19970800318<\/a>.<\/li>\n
L. Ruzicka, M. Pfeiffer (1933). “\u00dcber Jasminriechstoffe I. Die Konstitution des Jasmons”.\u00a0Helvetica Chimica Acta<\/a><\/em>\u00a016<\/strong>: 1208\u20131214.\u00a0doi<\/a>:10.1002\/hlca.193301601153<\/a>.<\/li>\n<\/ul>\n
<\/p>\n
Predict NMR spectrum<\/a><\/span><\/strong><\/p>\n
<\/p>\n\n\n\n\n\n
Formula:<\/big><\/td>\n C10H14O<\/big><\/td>\n<\/tr>\n
CAS#:<\/big><\/td>\n 488-10-8<\/big><\/td>\n<\/tr>\n
MW:<\/big><\/td>\n 150.22<\/big><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
<\/p>\n
$\"\"$ <\/span><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"
Jasmone\u00a0is a natural\u00a0organic compound\u00a0extracted from the volatile portion of the oil fromjasmine\u00a0flowers. It is a colorless to pale yellow liquid that has the odor of jasmine. Jasmone can exist in two\u00a0isomeric\u00a0forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone. The natural extract contains only the cis form, while synthetic material is often… Continue reading cis z jasmone<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"_links":{"self":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269"}],"collection":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/comments?post=269"}],"version-history":[{"count":9,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269\/revisions"}],"predecessor-version":[{"id":296,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269\/revisions\/296"}],"wp:attachment":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/media?parent=269"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/categories?post=269"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/tags?post=269"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Formula:<\/big><\/td>\n	C10H14O<\/big><\/td>\n<\/tr>\n
CAS#:<\/big><\/td>\n	488-10-8<\/big><\/td>\n<\/tr>\n
MW:<\/big><\/td>\n	150.22<\/big><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n <\/p>\n $\"\"$ <\/span><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":" Jasmone\u00a0is a natural\u00a0organic compound\u00a0extracted from the volatile portion of the oil fromjasmine\u00a0flowers. It is a colorless to pale yellow liquid that has the odor of jasmine. Jasmone can exist in two\u00a0isomeric\u00a0forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone. The natural extract contains only the cis form, while synthetic material is often… Continue reading cis z jasmone<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"_links":{"self":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269"}],"collection":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/comments?post=269"}],"version-history":[{"count":9,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269\/revisions"}],"predecessor-version":[{"id":296,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/posts\/269\/revisions\/296"}],"wp:attachment":[{"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/media?parent=269"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/categories?post=269"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/amcrasto.theeurekamoments.com\/wp-json\/wp\/v2\/tags?post=269"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}