40162-97-8 Usage
Organic compound
Used as a monomer in the production of polymers and as a crosslinking agent for polymers such as natural and synthetic rubbers
Appearance
Colorless to pale yellow liquid with a pungent odor
Reactivity
Highly reactive due to the presence of allyl groups in its structure
Uses
Reactant in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
Safety precautions
Can cause skin and eye irritation, potential for inhalation and ingestion hazards, handle with care.
Check Digit Verification of cas no
The CAS Registry Mumber 40162-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,6 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40162-97:
(7*4)+(6*0)+(5*1)+(4*6)+(3*2)+(2*9)+(1*7)=88
88 % 10 = 8
So 40162-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H17N/c1-3-6-10(7-4-2)8-5-9-11-10/h3-4,11H,1-2,5-9H2
40162-97-8Relevant articles and documents
Weinreb,Semmelhack
, p. 158,166 (1975)
Direct construction of quaternary carbon center utilizing an allylsamarium bromide reagent
Li, Zhifang,Zhang, Yongmin
, p. 5301 - 5306 (2007/10/03)
Direct geminal diallylation of lactones, lactams and acyclic amides containing a N-H bond has been achieved in the presence of allylsamarium bromide. By applying this method, quaternary carbons have been constructed, and 2,2-diallylated cyclic ethers, 2,2-diallylated nitrogen heterocycles and diallylated amides were synthesized in moderate to good yields under mild conditions.
A convenient synthesis of 2,2-diallylated nitrogen heterocycles by allylboration of lactams
Bubnov, Yuri N.,Pastukhov, Fedor V.,Yampolsky, Ilia V.,Ignatenko, Anatoli V.
, p. 1503 - 1505 (2007/10/03)
Lactams containing an N-H bond are smoothly transformed into 2,2- diallylated nitrogen heterocycles on heating with allylic boranes in THF followed by deboronation.
