CAS 112-77-6

oleoyl chloride

Description:

Oleoyl chloride, with the CAS number 112-77-6, is an acyl chloride derived from oleic acid. It is characterized by its long carbon chain, consisting of 18 carbon atoms with a cis double bond at the ninth position, which contributes to its unsaturated nature. Oleoyl chloride is a colorless to pale yellow liquid with a pungent odor, typical of acyl chlorides. It is highly reactive, particularly with water, leading to the formation of oleic acid and hydrochloric acid upon hydrolysis. This reactivity makes it useful in organic synthesis, particularly in the formation of amides and esters. Oleoyl chloride is soluble in organic solvents such as chloroform and ether but is insoluble in water due to its hydrophobic nature. Safety precautions are necessary when handling this compound, as it can cause severe irritation to the skin, eyes, and respiratory tract. Overall, oleoyl chloride is an important intermediate in the synthesis of various chemical compounds, particularly in the fields of pharmaceuticals and agrochemicals.

Formula: C₁₈H₃₃ClO

InChI: InChI=1S/C18H33ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3/b10-9-

InChI key: InChIKey=MLQBTMWHIOYKKC-KTKRTIGZSA-N

SMILES: C(C/C=C\CCCCCCCC)CCCCCC(Cl)=O

Synonyms:

• (9Z)-1-chlorooctadec-9-ene
• (9Z)-9-Octadecenoyl chloride
• (9Z)-octadec-9-enoyl chloride
• (Z)-9-Octadecenoyl chloride
• 9-(Z)-Octadecen-1-oyl chloride
• 9-Octadecenoyl chloride, (9Z)-
• 9-Octadecenoyl chloride, (Z)-
• 9-Octadecenoyl chloride, (Z)- (9CI)
• Nsc 97299
• Octadec-9-Enoyl Chloride
• Oleic acid chloride
• Oleic chloride
• Oleyl chloride
• cis-9-Octadecenoyl chloride
• Oleoyl chloride
• Oleoyl chloride
• 9-OCTADECENOYL CHLORIDE
• (z)-9-octadecenoylchlorid
• oleoylchloride,(mixturewithca.35-40%elaidicacidchloride)
• OLEOYL CHLORIDE, TECH., 85%
• OCTADECENOYLCHLORIDE
• (Z)-9-Octadecenoic acid chloride
• techn,mixturewithca.35-40%Elaidicacidchloride
• (Z)-9-Octadecenoylchloride
• DELTA 9 CIS-OCTADECENOYL CHLORIDE
• [(9Z)-1-Oxo-9-octadecenyl] chloride
• Oleoyl

Oleoyl Chloride

CAS: 112-77-6

Formula: C₁₈H₃₃ClO

Purity: >80.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 300.91

Ref: 3B-O0053

OLEIC ACID CHLORIDE

CAS: 112-77-6

Formula: C₁₈H₃₃ClO

Purity: 80%

Color and Shape: Liquid

Molecular weight: 300.9070

Ref: IN-DA003TH9

Oleoyl chloride

CAS: 112-77-6

Formula: CH₃(CH₂)₇CHCH(CH₂)₇COCl

Molecular weight: 300.91

Ref: 7W-GK2229

Oleoyl Chloride

CAS: 112-77-6

Oleoyl Chloride

Purity: 90%

Molecular weight: 300.91g/mol

Ref: 54-OR1029964

9(Z)-Octadecenoyl chloride

CAS: 112-77-6

Formula: C18H33ClO

Purity: >99%

Color and Shape: Liquid

Molecular weight: 300.91

Ref: 48-46-1801

Oleoyl Chloride

CAS: 112-77-6

Purity: 80%

Molecular weight: 300.9100037

Ref: 10-F626276

Oleoyl Chloride

Controlled Product

CAS: 112-77-6

Stability Moisture Sensitive
Applications Oleyl Chloride is used as a chemical reagent in the preparation of Vitamin E analogs as well as antiviral nucleoside phosphoramidate prodrugs used in the treatment of HIV and HBV.
References Cho, J. et al.: Bioorg. Med. Chem., 22, 6665 (2014); Iwata, R. et al.: Bioorg. Med. CHem. Lett., 25, 815 (2015);

Formula: C₁₈H₃₃ClO

Color and Shape: Neat

Molecular weight: 300.907

Ref: TR-O526750

Oleoyl chloride

CAS: 112-77-6

Oleoyl chloride is a monosodium salt of oleic acid. It is a biocompatible polymer that has been shown to have antimicrobial properties and has been used as a natural drug in the treatment of microbial infections. Oleoyl chloride inhibits bacterial growth by binding to receptors on the surface of cells, especially those with high resistance to antibiotics. Oleoyl chloride has been found to be effective against Gram-positive bacteria, such as vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus (MRSA), and Gram-negative bacteria, such as Salmonella enterica serovar Typhimurium. Oleoyl chloride also has anti-inflammatory properties that are related to its ability to inhibit the production of prostaglandins. This compound can be synthesized from natural compounds containing nitrogen atoms, such as amino acids and proteins, and hydroxyl groups, such as alcohols.

Formula: C₁₈H₃₃ClO

Purity: Min. 95%

Molecular weight: 300.91 g/mol

Ref: 3D-FO172746