50816-18-7

Basic information

• Product Name: ACETIC ACID 9-DECEN-1-YL ESTER
• Synonyms: Acetic acid 9-decenyl ester;aceticacid,9-decenylester;aceticaciddecenylester;Decenyl acetate;decenylacetate;9-DECEN-1-OL ACETATE;9-DECEN-1-YL ACETATE;9-DECENYL ACETATE
• CAS NO: 50816-18-7
• Molecular Formula: C₁₂H₂₂O₂
• Molecular Weight: 198.3
• EINECS: 256-784-1
• Mol File: 50816-18-7.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 246°C
• Appearance: /
• Density: 0,88 g/cm3
• Refractive Index: 1.4350-1.4380
• CAS DataBase Reference: ACETIC ACID 9-DECEN-1-YL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: ACETIC ACID 9-DECEN-1-YL ESTER(50816-18-7)
• EPA Substance Registry System: ACETIC ACID 9-DECEN-1-YL ESTER(50816-18-7)

Safety Data

• Safety Statements: 24/25
• RTECS: AG5230000
• Hazardous Substances Data: 50816-18-7(Hazardous Substances Data)

Usage

Safety Profile

Low toxicity by ingestion and skin contact. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Upstream product

• 26118-61-6 1,10-decanediol diacetate 
• 29541-97-7 9-acetoxynonal 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 5009-33-6 1-dodecen-11-one 
• 13019-22-2 9-Decen-1-ol 
• 108-24-7 acetic anhydride 
• 35153-15-2 (Z)-9-tetradecen-1-ol 
• 141-78-6 ethyl acetate 
• 75-36-5 acetyl chloride 
• 85576-23-4 1-Chloro-8-(1-ethoxy-ethoxy)-octane 
• 74-86-2 acetylene 
• 56904-95-1 (bromo-8 octyloxy-1)-1, ethoxy-1 ethane 
• 85576-11-0 C₁₃H₂₅LiO₂ 
• 581-55-5 benzylidene 1,1-diacetate 

Downstream Products

• 13019-22-2 9-Decen-1-ol 
• 74-85-1 ethene 
• 61319-25-3 9-tetradecyn-1-yl acetate 
• 57568-18-0 diacetoxy-1,8 octadecene-9 
• 16725-53-4 (Z)-9-tetradecen-1-yl acetate 
• 23192-82-7 (E)-tetradec-9-en-1-yl acetate 
• 33189-72-9 (E)-tetradec-11-en-1-yl acetate 
• 56218-69-0 (E)-9-hexadecenyl acetate 
• 19754-58-6 2-dec-9-ynyloxy-tetrahydro-pyran 
• 60037-69-6 9-tetradecyn-1-ol 
• 17643-36-6 9-decyn-1-ol 
• 88109-73-3 9-hexadecyn-1-ol 
• 19754-59-7 tetrahydro-2-(9-tetradecynyloxy)pyran 
• 1286209-77-5 C₂₂H₃₄O₅ 

Relevant articles and documents

New SF5-long chain carbon systems

A new SF5-terminated perfluoroalkyl thiol - SF5(CF2)6CH2CH2SH - and a symmetric SF5-terminated dialkyl disulfide - [SF5CH-CH(CH2)8S]2 - were synthesized from the corresponding SF5-terminated precursors. The chemistry employed in the preparation of the disulfide encompasses high yield pathways for the preparation of new SF5-long chain derivatives.

Amine-borane complex-initiated SF5Cl radical addition on alkenes and alkynes

The SF5Cl radical addition on unsaturated compounds was performed using an air-stable amine-borane complex as the radical initiator. This method showed to be complementary to the classic Et3B-mediated SF5Cl addition on alkenes and alkynes. A total of seven alkene and three alkyne derivatives were tested in the reaction, with yields ranging from 3% to 85%.

Ethyl acetate as an acetyl surrogate for the iodine catalyzed acetylation of alcohols

The use of readily available ethyl acetate in the presence of iodine as an alternative acetylating agent is reported. Amines and phenols were unreactive under the examined reaction conditions, indicating that the method is highly chemoselective.