6974-87-4

Basic information

• Product Name: ETHYL A-BROMOLAURATE
• Synonyms: ETHYL A-BROMOLAURATE;ETHYL ALPHA-BROMO LAURATE;Ethyl 2-bromo dodecanoate (Laurate);α-Bromo-dodecanoic acid ethyl ester;2-Bromododecanoic acid ethyl ester;Ethyl2-bromoLaurate;ALPHA-BROMO-DODECANOIC ACID ETHYL ESTER;2-Bromolauric acid ethyl ester
• CAS NO: 6974-87-4
• Molecular Formula: C₁₄H₂₇BrO₂
• Molecular Weight: 307.27
• EINECS: 230-227-2
• Mol File: 6974-87-4.mol

Chemical Properties

• Boiling Point: 300.8°C at 760 mmHg
• Flash Point: 150.7°C
• Appearance: /
• Density: 1.11g/cm³
• Vapor Pressure: 0.0011mmHg at 25°C
• Refractive Index: 1.464
• CAS DataBase Reference: ETHYL A-BROMOLAURATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL A-BROMOLAURATE(6974-87-4)
• EPA Substance Registry System: ETHYL A-BROMOLAURATE(6974-87-4)

Safety Data

• Hazardous Substances Data: 6974-87-4(Hazardous Substances Data)

Usage

Uses

Used in Cosmetic and Personal Care Industry:
ETHYL A-BROMOLAURATE is used as an ingredient in the production of various cosmetic and personal care products such as soaps, shampoos, and lotions. It serves to enhance the texture and performance of these products, providing a pleasant sensory experience for the user.
Used as a Fragrance Ingredient:
In the fragrance industry, ETHYL A-BROMOLAURATE is used to impart a pleasant, fruity aroma to a variety of products. Its aromatic properties make it a valuable component in creating appealing scents for consumer goods.
Used as a Flavoring Agent in Food Products:
ETHYL A-BROMOLAURATE is also utilized in the food industry as a flavoring agent. Its fruity aroma adds a desirable taste and scent to food products, enhancing the overall sensory experience for consumers.
Used as an Intermediate in Organic Synthesis:
Due to its versatile chemical properties, ETHYL A-BROMOLAURATE is often used as an intermediate in the synthesis of other organic compounds. This makes it a valuable component in the production of various chemical products and intermediates for different industries.

InChI:InChI=1/C14H27BrO2/c1-3-5-6-7-8-9-10-11-12-13(15)14(16)17-4-2/h13H,3-12H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 111-56-8 2-bromododecanoic acid 
• 143-07-7 lauric acid 
• 617-33-4 ethyl dibromoacetate 
• 1188-96-1 tridecylborane 

Downstream Products

• 334-48-5 1-decanoic acid 
• 112-37-8 undecylenic acid 
• 63538-36-3 2-{4-[4-(1-Ethoxycarbonyl-undecyloxy)-phenoxy]-phenoxy}-dodecanoic acid ethyl ester 
• 51337-98-5 2-[4-(4-Chloro-phenoxy)-phenoxy]-dodecanoic acid ethyl ester 
• 40843-13-8 4-(4-Chlorphenoxy)-α-phenoxy-laurinsaeure 
• 31558-67-5 2-(5,6,7,8,8a,9-Hexahydro-4bH-fluoren-2-ylsulfanyl)-dodecanoic acid ethyl ester 
• 27747-69-9 2-(9H-Fluoren-2-ylsulfanyl)-dodecanoic acid ethyl ester 
• 188699-87-8 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-dodecanoic acid ethyl ester 
• 63538-47-6 2-{4-[4-(1-Carboxy-undecyloxy)-phenoxy]-phenoxy}-dodecanoic acid 
• 38798-98-0 α-[p-(1-cyclohexenyl)-phenoxy]-dodecanoic acid ethyl ester 
• 2530-33-8 Decylsuccinic acid 
• 35237-37-7 2-amino-dodecanoic acid 
• 161459-64-9 C₄₃H₅₄N₂O₉ 

Relevant articles and documents

Unnatural nucleosides and nucleotides. III. Preparation of 2-14C and 4-14C labelled 5-alkyluracils and 5-alkyl-2'-deoxyuridines

2-14C Labelled 5-alkyluracils were prepared by condensation of the diethylacetals of α-formyl-carbonic acid esters with 14C-thiourea. Compounds labelled at 4-C were synthesized by condensation of the labelled carboxylic acid derivatives with thiourea. β-Anomers of 5-alkyl-2'-deoxyuridines were obtained in a fairly good radiochemical yield. Alkyl substituents ranged from methyl to tetradecyl, isopropyl and tert-butyl.