64437-48-5 Usage
Molecular structure
Long-chain unsaturated alcohol with a double bond at the 10th carbon atom
Physical state
Colorless, waxy solid at room temperature
Odor
Slight floral odor
Natural sources
Found in plants, fruits, and vegetables
Flavors and fragrances
Used in the production of various flavors and fragrances
Cosmetics and personal care products
Used in the formulation of cosmetics and personal care products
Pharmaceutical industry
Has potential applications due to its biological activities and therapeutic properties
Versatility
Wide range of uses in different industries
Biological activities
Exhibits various biological activities, which contribute to its potential therapeutic properties
Therapeutic properties
Possesses potential therapeutic properties, making it a compound of interest in the pharmaceutical industry
Check Digit Verification of cas no
The CAS Registry Mumber 64437-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,3 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64437-48:
(7*6)+(6*4)+(5*4)+(4*3)+(3*7)+(2*4)+(1*8)=135
135 % 10 = 5
So 64437-48-5 is a valid CAS Registry Number.
64437-48-5Relevant articles and documents
Industrial synthesis method of dichocrocis punctiferalis sex pheromone
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Paragraph 0029-0042, (2020/06/30)
The invention belongs to the field of chemical synthesis, and particularly relates to an industrial synthesis method of a dichocrocis punctiferalis sex pheromone. The method comprises the following steps: taking 1, 10-decanediol as a raw material; carrying out a single-side bromination reaction to prepare 10-bromodecanol; then reacting the 10-bromodecanol with triphenylphosphine to obtain 10-hydroxydecyltriphenylphosphine salt; performing a Wittig reaction with n-hexaldehyde under the action of alkali to obtain cis-based 10-hexadecene-1-ol; performing isomerization on the cis-based enol underthe action of p-methylthiophenol to obtain trans-based 10-hexadecene-1-ol; and finally performing oxidation under the action of an oxidant to obtain the final product 10-hexadecenal. The method is mild in reaction condition and suitable for large-scale production.
IMMUNOTHERAPEUTIC AGENT
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Paragraph 0101-0102, (2018/07/29)
Compounds for use in the treatment of sepsis and/or the prevention or treatment of post-sepsis syndrome.
