16745-94-1 Usage
General Description
3,4-Dimethyl-1-hexene is a chemical compound with the formula C8H16. It is a colorless liquid with a strong odor and is commonly used as a reactant in organic synthesis. This chemical is classified as an alkene, which means it contains a carbon-carbon double bond. It is often used as a starting material for the synthesis of other organic compounds, particularly in the production of fragrances and flavorings. 3,4-Dimethyl-1-hexene is also used in the manufacturing of plasticizers and as a solvent in various industrial processes. It is important to handle this chemical with caution, as it can be flammable and may cause irritation to the skin and eyes upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 16745-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16745-94:
(7*1)+(6*6)+(5*7)+(4*4)+(3*5)+(2*9)+(1*4)=131
131 % 10 = 1
So 16745-94-1 is a valid CAS Registry Number.
16745-94-1Relevant articles and documents
Copper catalyzed magnesium-Barbier reaction for γ-selective alkyl-allyl coupling
Erdik, Ender,Ko?o?lu, Melike
, p. 4211 - 4214 (2008/02/08)
CuCN catalyzed alkyl-allyl coupling under magnesium-Barbier conditions occurs regioselectively and affords predominantly the γ-products in good to high yields. This one-pot CuCN catalyzed reaction utilising Mg, an alkyl halide and an allylic substrate in THF at room temperature provides an easy alternative to the classical CuCN catalyzed γ-allylation of alkyl Grignard reagents.
THERMISCHE STABILITAET VON BIS(ALK-2-ENYL)ZINK-VERBINDUNGEN
Lehmkuhl, Herbert,Doering, Ingo,Nehl, Hans
, p. 7 - 12 (2007/10/02)
The dialk-2-enylzinc compounds I-III react slowly at 20 to 50 deg C by addition of the Zn-C bond to the C=C bond of an alk-2-enyl group to give oligomers from which the alkenes XIII-XV are released on hydrolysis.For I-III homolytic cleavage of the Zn-Callyl bond, followed by coupling of the allyl radicals to give the alkadienes V-VII, IX and XI predominates above 50 deg C.IV decomposes mainly homolytically even at 20 deg C.