Oleoyl Chloride Oleoyl Chloride

Structural formula

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

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,1.46Kpa）：200

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