120293-93-8 Usage
Description
Methyl 6,7-10,11-bis(epoxy)-3,7,11-trimethyl-2-dodecenoate is a complex organic compound with a unique molecular structure featuring multiple epoxy and methyl groups. It is characterized by its epoxy groups at positions 6,7 and 10,11, and methyl groups at positions 3,7, and 11. methyl 6,7-10,11-bis(epoxy)-3,7,11-trimethyl-2-dodecenoate has a long carbon chain with a terminal double bond, which may confer specific chemical properties and reactivity.
Uses
Used in Chemical Synthesis:
Methyl 6,7-10,11-bis(epoxy)-3,7,11-trimethyl-2-dodecenoate is used as a key intermediate in the synthesis of various specialty chemicals and pharmaceuticals. Its unique structure allows for targeted functionalization and the creation of complex molecules with specific biological activities.
Used in Coatings and Adhesives Industry:
In the coatings and adhesives industry, this compound is used as a reactive diluent for epoxy resins. Its epoxy groups can cross-link with other epoxy resins, improving the mechanical properties and durability of the final product.
Used in Polymer Science:
Methyl 6,7-10,11-bis(epoxy)-3,7,11-trimethyl-2-dodecenoate is utilized in polymer science as a monomer for the synthesis of polymers with tailored properties. The presence of multiple reactive sites allows for the creation of polymers with specific characteristics, such as improved thermal stability or enhanced mechanical strength.
Used in Flavor and Fragrance Industry:
Due to its complex structure, methyl 6,7-10,11-bis(epoxy)-3,7,11-trimethyl-2-dodecenoate may also find applications in the flavor and fragrance industry, where it could be used to create unique scents or flavors.
Used in Pest Control:
Given its complex structure and potential reactivity, this compound could be explored for use in the development of novel pesticides or insecticides, where it may act as a growth regulator or disrupt the hormonal balance in pests.
Check Digit Verification of cas no
The CAS Registry Mumber 120293-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,9 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120293-93:
(8*1)+(7*2)+(6*0)+(5*2)+(4*9)+(3*3)+(2*9)+(1*3)=98
98 % 10 = 8
So 120293-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H26O4/c1-11(10-14(17)18-5)6-7-13-16(4,20-13)9-8-12-15(2,3)19-12/h10,12-13H,6-9H2,1-5H3/b11-10+
120293-93-8Relevant articles and documents
Ichinose,I. et al.
, p. 605 - 607 (1978)
An efficient asymmetric synthesis of the higher dipteran juvenile hormone III bisepoxide
Rickards, Rodney W.,Thomas, Richard D.
, p. 8369 - 8372 (2007/10/02)
(2E,6S,7S,10R) - Juvenile hormone III bisepoxide, the putative characteristic juvenile hormone of higher dipteran insects, has been synthesised efficiently and in high stereochemical purity from geraniol by application of Sharpless asymmetric epoxidation and dihydroxylation procedures.
Synthesis of four stereoisomers of the higher dipteran juvenile hormone III bisepoxide
Rickards, Rodney W.,Thomas, Richard D.
, p. 8137 - 8140 (2007/10/02)
The 6S,7S,10R-, 6S,7S,10S-, 6R,7R,10S-, and 6R,7R,10R-stereoisomers of the juvenile hormone III bisepoxide from higher Dipteran insects have been synthesised in high stereoisomeric purity. The route involves Sharpless epoxidation of geraniol to enantiomeric epoxyalcohols, which are each elaborated via separable diastereomeric bromohydrins.
