Toluene diisocyanate manufacturer Knowledge Oleoyl Chloride Oleoyl Chloride

Oleoyl Chloride Oleoyl Chloride

Oleoyl chloride structural formula

Structural formula

Business number 036M
Molecular formula C18H33ClO
Molecular weight 300.91
label

9-Octadecenoyl chloride,

(Z)-9-Octadecenoylchloride,

detergent,

aliphatic compounds

Numbering system

CAS number:112-77-6

MDL number:MFCD00134332

EINECS number:204-005-0

RTECS number:None

BRN number:1211748

PubChem number:24897935

Physical property data

1. Characteristics: Liquid.


2. Density (g/mL,20):0.912


3. Relative vapor density ( g/mL,Air=1): Undetermined


4. Melting point (ºC): -46


5. Boiling point (ºC,normal pressure): Undetermined


6. Boiling point (ºC,1.46Kpa200


7. Refractive index:1.463


8. Flashpoint (ºC):110


9. Specific optical rotation (º): Undetermined


10. Autoignition point or ignition temperature (ºC): Undetermined


11. Vapor pressure (mmHg,ºC): Undetermined


12. Saturated vapor pressure (kPa, ºC): Undetermined


13. Heat of combustion (KJ/mol): Undetermined


14. Critical temperature (ºC): Undetermined


15. Critical pressure (KPa): Undetermined


16.


4. Rotatable Number of chemical bonds: 15


5. Interchange Number of isomers:


6. Topological molecules Polar surface area (TPSA):17.1


7. Heavy atoms Quantity: 20


8. Surface charge :0


9. Complexity :236


10. Number of isotope atoms:0


11. Determine the number of atomic stereocenters:0


12. Uncertain number of atomic stereocenters:0


13. Determine the number of stereocenters of chemical bonds:1


14. Uncertain number of chemical bond stereocenters:0


15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

Originated from the reaction of oleic acid and phosphorus trichloride. Put oleic acid into the reaction pot, slowly add phosphorus trichloride while stirring, and control the feeding temperature at 25-33 ℃. After addition, heat up to55℃, insulate 4h and then separate the lower layer of phosphorous acid to obtain oleoyl chloride.

Purpose

Used as an intermediate in organic synthesis. Use oleoyl chloride to acylate 2-sulfo -4- aminoanisole to obtain a cleaning agent

18.0pt; mso-para-margin-left: -.01gd” align=left>10. Isotopes Number of atoms: 0


11. Determine the number of atomic stereocenters:0


12. Uncertain number of atomic stereocenters:0


13. Determine the number of stereocenters of chemical bonds:1


14. Uncertain number of chemical bond stereocenters:0


15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

Originated from the reaction of oleic acid and phosphorus trichloride. Put oleic acid into the reaction pot, slowly add phosphorus trichloride while stirring, and control the feeding temperature at 25-33 ℃. After addition, heat up to55℃, insulate 4h and then separate the lower layer of phosphorous acid to obtain oleoyl chloride.

Purpose

Used as an intermediate in organic synthesis. Use oleoyl chloride to acylate 2-sulfo -4- aminoanisole to obtain a cleaning agent

AMILY: 宋体; mso-bidi-font-family: ‘Times New Roman’; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi -language: AR-SA”>Used as an intermediate in organic synthesis. Use oleoyl chloride to convert 2-sulfo-4- Cleaning agent can be obtained by acylation reaction of aminoanisole

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/26673

author:

Previous article
Next article
Contact Us

Contact us

+86 - 152 2121 6908

Online consultation: QQ交谈

E-mail: sales@newtopchem.com

Working hours: Monday to Friday, 9:00-17:30, closed on holidays
Follow wechat
Scan wechat and follow us

Scan wechat and follow us

Follow Weibo
Back to top
Home
E-mail
Products
Search