2350-24-5 Usage
Type of compound
Chlorinated alkane
Carbon chain length
Seven-carbon chain
Methyl group position
Fifth position
Physical state
Colorless liquid
Odor
Faint, sweet
Solubility
Insoluble in water, soluble in organic solvents
Uses
Organic synthesis, intermediate in production of other chemical compounds, solvent, reactant in manufacturing of pharmaceuticals, agrochemicals, and specialty chemicals
Safety precautions
Harmful if inhaled, ingested, or absorbed through the skin, may cause irritation to respiratory system and skin, store in a cool, dry place, and keep away from sources of heat or ignition.
Check Digit Verification of cas no
The CAS Registry Mumber 2350-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2350-24:
(6*2)+(5*3)+(4*5)+(3*0)+(2*2)+(1*4)=55
55 % 10 = 5
So 2350-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Cl/c1-3-8(2)6-4-5-7-9/h8H,3-7H2,1-2H3
2350-24-5Relevant articles and documents
New syntheses of 1,7-dimethylnonyl propanoate, the western corn rootworm pheromone, in four different ways via cross metathesis, alkylation and coupling reactionsss
Mori, Kenji
, p. 595 - 600 (2011/04/23)
A mixture of the four stereoisomers of 1,7-dimethylnonyl propanoate, the female sex pheromone of the western corn rootworm (Diabrotica virgifera virgifera LeConte), was synthesized in four different ways by employing one of the following four reactions as the key step: (i) cross metathesis using the Grubbs I catalyst, (ii) cross metathesis using the Grubbs II catalyst, (iii) alkylation of an alkynide anion, and (iv) Grignard coupling in the presence of dilithium tetrachlorocuprate. Although the cross metathesis approaches enabled two short syntheses (4 or 6 steps) of the pheromone to be achieved, the cheapest and most efficient synthesis was possible via Grignard coupling to give the desired pheromone in a 40% overall yield based on 2-methyl-1-butanol (8 steps).
