67952-61-8 Usage
Alkene
Yes
Bromine atom position
First position
Explanation
The bromine atom is attached to the first carbon atom in the 1-bromoundec-2-ene molecule.
Explanation
The carbon-carbon double bond in 1-bromoundec-2-ene is located between the second and third carbon atoms in the molecule.
Explanation
1-bromoundec-2-ene is known for its reactivity in various chemical reactions, including addition, substitution, and elimination reactions.
Explanation
Due to its versatile nature, 1-bromoundec-2-ene is used as an important intermediate in the production of various chemicals and pharmaceuticals. It is also utilized in the production of polymers and surfactants.
Explanation
1-bromoundec-2-ene plays a significant role in the industrial and research sectors due to its wide range of applications and its ability to be used as a starting material for the synthesis of various compounds.
Double bond location
Between the second and third carbon atoms
Reactivity
High
Applications
Organic synthesis, polymers, surfactants, and pharmaceuticals
Industrial and research importance
High
Check Digit Verification of cas no
The CAS Registry Mumber 67952-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,5 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67952-61:
(7*6)+(6*7)+(5*9)+(4*5)+(3*2)+(2*6)+(1*1)=168
168 % 10 = 8
So 67952-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H21Br/c1-2-3-4-5-6-7-8-9-10-11-12/h9-10H,2-8,11H2,1H3/b10-9+
67952-61-8Relevant academic research and scientific papers
Highly selective hydrosilylation of equilibrating allylic azides
Liu, Ruzhang,Liu, Yongmei,Wang, Juan,Wei, Zhen,Xue, Huaiguo
supporting information, p. 5038 - 5041 (2020/05/18)
The Pt-catalyzed hydrosilylation of equilibrating allylic azides is reported. The reaction provides only one out of four possible hydrosilylation products in good yields and with very high chemoselectivity (alk-1-enevs.alk-2-ene), regioselectivity (linearvs.branched), and excellent functional group tolerance.
An efficient method for conversion of 1-alken-3-yl carbonates to 1- alkenes and 3-chloro-1-alkenes via allyltitaniums
Matsuda, Shin-Ichiro,An, Duk Keun,Okamoto, Sentaro,Sato, Fumie
, p. 7513 - 7516 (2007/10/03)
Hydrolysis and halogenolysis of the allyltitaniums derived from allylic carbonates and a Ti(O-i-Pr)4/2 i-PrMgCl reagent proceed with high regio- and stereoselectivity, thus providing an efficient method for converting 1- alken-3-yl carbonates to 1-alkenes or 3-chloro-1-alkenes.
A New and Efficient One-Pot Preparation of Alkyl Halides From Alcohols
Camps, Francisco,Gasol, Vicens,Guerrero, Angel
, p. 511 - 512 (2007/10/02)
Primary alkanols and 2-alkenols are converted into the corresponding halides in high yield by a one-pot, two-step reaction via transformation into intermediate trifluoroacetates followed by nucleophilic substitution with lithium halides.
