15306-27-1 Usage
Description
1-Heptacosene is a long-chain hydrocarbon compound belonging to the class of alkenes, which are organic molecules characterized by a carbon-carbon double bond. It is a colorless, waxy solid at room temperature and is commonly found in various plant and animal species as a part of their pheromones, which are chemical signals used for communication between individuals of the same species.
Uses
Used in Insect Communication:
1-Heptacosene is used as a chemical signal for insect communication, particularly in the mating behaviors of certain insect species. It plays a crucial role in attracting and signaling between insects of the same species.
Used in Plant Protection:
1-Heptacosene is used as a component of the cuticular lipids in some plants, where it contributes to the waxy coating on leaves and stems. This helps reduce water loss and protect against environmental stress.
Used in Organic Synthesis and Material Science:
1-Heptacosene is used as a long hydrophobic hydrocarbon chain in the field of organic synthesis and material science. Its structure may be useful for creating surfactants and polymer materials.
Check Digit Verification of cas no
The CAS Registry Mumber 15306-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,0 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15306-27:
(7*1)+(6*5)+(5*3)+(4*0)+(3*6)+(2*2)+(1*7)=81
81 % 10 = 1
So 15306-27-1 is a valid CAS Registry Number.
15306-27-1Relevant articles and documents
Convenient Synthesis of 4-Acetyl-2-methoxy-5-methyl-triacontane and 23-Hydroxytriacontan-2-one, the Constituents of Curculigo orchioides
Iyer, R.,Mamdapur, V. R.,Chadha, M. S.
, p. 887 - 890 (2007/10/02)
Unambiguous syntheses of the two title compounds (I) and (II), recently isolated by Mehta et al. and Misra et al. from Curculigo orchioides are reported.The syntheses use the Grignard coupling of undecenyl bromide with cetyl bromide (2) and monobromo pyranyl ether (10) of dodecanediol, respectively as one of the key reactions.Further elaboration of the products in each case leads to the desired compounds (I) and (II).Complete identity of the synthetic products with the natural ones, however, could not be established.
