13043-66-8 Usage
General Description
(Z)-1,1-diethoxytridec-2-ene is a chemical compound with the molecular formula C15H30O2. It is a colorless liquid with a molecular weight of 242.40 g/mol. (Z)-1,1-diethoxytridec-2-ene is categorized as an unsaturated organic compound, containing a double bond between carbon atoms. It is commonly used in organic synthesis and industrial applications as a reagent for various chemical reactions. (Z)-1,1-diethoxytridec-2-ene has also been studied for its potential use in pharmaceutical and agrochemical industries due to its unique chemical properties. However, it is important to handle this compound with caution, as it can be hazardous if not properly handled and stored.
Check Digit Verification of cas no
The CAS Registry Mumber 13043-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13043-66:
(7*1)+(6*3)+(5*0)+(4*4)+(3*3)+(2*6)+(1*6)=68
68 % 10 = 8
So 13043-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O2/c1-4-7-8-9-10-11-12-13-14-15-16-17(18-5-2)19-6-3/h15-17H,4-14H2,1-3H3/b16-15-
13043-66-8Relevant articles and documents
Ruthenium-catalysed Z-selective cross metathesis of allylic-substituted olefins
Quigley, Brendan L.,Grubbs, Robert H.
, p. 501 - 506 (2014)
The Z-selective cross metathesis of allylic-substituted olefins is explored with recently developed ruthenium-based metathesis catalysts. The reaction proceeds with excellent stereoselectivity for the Z-isomer (typically >95%) and yields of up to 88% for a variety of allylic substituents. This includes the first synthesis of Z-α,β-unsaturated acetals by cross metathesis and their elaboration to Z-α,β-unsaturated aldehydes. In addition, the reaction is tolerant of a variety of cross partners, varying in functionality and steric profile.
