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58763-68-1

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58763-68-1 Usage

Description

(E)-dodec-7-en-9-ynol, also known as 2-(7-dodecenyl)-1-propanol, is a chemical compound with a molecular formula of C12H22O. It is a colorless liquid characterized by a sweet, floral odor. (E)-dodec-7-en-9-ynol is not only synthesized for various applications but also occurs naturally in plants and has been identified as a component of pheromones in certain species, such as the African armyworm moth. Its versatility is evident in its usage across different industries, including the fragrance, food, pharmaceutical, and agricultural sectors.

Uses

Used in the Fragrance Industry:
(E)-dodec-7-en-9-ynol is used as a perfume ingredient for its sweet, floral scent, contributing to the creation of various fragrances in the perfumery market.
Used in the Food Industry:
As a flavoring agent, (E)-dodec-7-en-9-ynol enhances the taste and aroma of food products, providing a pleasant sensory experience for consumers.
Used in the Pharmaceutical Industry:
(E)-dodec-7-en-9-ynol serves as a building block in the synthesis of other chemicals, which can be utilized for developing pharmaceutical products. Its antimicrobial and antioxidant properties also suggest potential applications in the development of new drugs or treatments.
Used in the Agricultural Industry:
Given its natural occurrence in plants and identification as a pheromone component, (E)-dodec-7-en-9-ynol may have applications in agricultural practices, such as pest control or enhancement of crop protection mechanisms.
Used as a Chemical Building Block:
(E)-dodec-7-en-9-ynol is used as a starting material for the synthesis of other chemicals, highlighting its importance in the chemical industry and the potential for further development of novel compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 58763-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58763-68:
(7*5)+(6*8)+(5*7)+(4*6)+(3*3)+(2*6)+(1*8)=171
171 % 10 = 1
So 58763-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h5-6,13H,2,7-12H2,1H3/b6-5+

58763-68-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dodec-7t-en-9-yn-1-ol

1.2 Other means of identification

Product number -
Other names (E)-Dodec-7-en-9-yn-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58763-68-1 SDS

58763-68-1Relevant articles and documents

Method for preparing trans -7 and cis -9 - dodecadiene acetate

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Paragraph 0045; 0050-0051; 0056; 0061-0062; 0067; 0072-0073, (2021/10/11)

The invention discloses a method for preparing trans -7 and cis -9 - dodecadiene acetate, which comprises (1) adding 1 - 1 dichloroethylene in 2 - butyne tetrahydrofuran solution. The metal palladium compound, cuprous iodide and diisopropylamine undergo a coupling reaction to obtain 1 - chlorine -3 - yne -1 - hexene. (2) 20 °C (ClMgO) Under stirring, at CH. 2 )6 In MgCl, hexamethylphosphoric acid triamide and ferric acetyl acetonate are sequentially added, 1 - chlorine -3 - yne -1 - hexene is added dropwise to obtain the trans 7 - dodecene -9 - alkynol. (3) Zn powder was added to trans 7 - dodecene -9 - alkynol, stirred to obtain trans 7, cis 9 - dodecadienol, acetic anhydride and pyridine were added and stirred to obtain trans -7, cis -9 - dodecadiene acetate. The method provided by the invention is cheap and wide in source; the method has the advantages of short synthesis period, less steps, high yield, good stereoselectivity and simple post-treatment.

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