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2-ethylhexyl bromoacetate is a chemical compound that belongs to the class of alkyl bromoacetates. It is commonly used as a reagent in organic synthesis and serves as a versatile building block for various organic compounds. This chemical is typically prepared by reacting 2-ethylhexanol with bromoacetyl bromide in the presence of a base. 2-ethylhexyl bromoacetate has a wide range of applications in the production of pharmaceuticals, fragrances, and other fine chemicals. It is known for its mild and selective reactivity, making it a valuable tool for chemical transformations in the laboratory setting. Additionally, it is considered to be relatively stable and safe to handle when proper precautions are taken.

68144-73-0

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68144-73-0 Usage

Uses

Used in Pharmaceutical Industry:
2-ethylhexyl bromoacetate is used as a reagent for the synthesis of various pharmaceutical compounds due to its mild and selective reactivity, which allows for efficient chemical transformations in the laboratory setting.
Used in Fragrance Industry:
2-ethylhexyl bromoacetate is used as a building block for the production of fragrances, contributing to the creation of unique and complex scents.
Used in Fine Chemicals Industry:
2-ethylhexyl bromoacetate is used as a versatile component in the synthesis of fine chemicals, enabling the development of high-quality specialty products.

Check Digit Verification of cas no

The CAS Registry Mumber 68144-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68144-73:
(7*6)+(6*8)+(5*1)+(4*4)+(3*4)+(2*7)+(1*3)=140
140 % 10 = 0
So 68144-73-0 is a valid CAS Registry Number.

68144-73-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylhexyl 2-bromoacetate

1.2 Other means of identification

Product number -
Other names 2-Ethylhexyl bromoacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:68144-73-0 SDS

68144-73-0Relevant academic research and scientific papers

WATER- OR ACID-TRIGGERED FRAGRANCE RELEASE FUNCTIONAL MONOMER AND POLYMER SYSTEM

-

Page/Page column 14, (2017/06/21)

A triggerable composition for one-stage, controlled release of a functional chemical includes a functional monomer having a structure selected from the group described herein, wherein R is a polymerizable portion, N+X- is a quaternar

Synthesis and biological evaluation of sulfur-containing cinnamate and salicylate derivatives

Chiang, Chih-Chia,Chang, Tsu-Chung,Tsai, Hou-Jen,Hsu, Ling-Yih

, p. 369 - 373 (2008/09/20)

UV irradiation induced formation of reactive oxygen radical species and matrix metalloproteinases (MMPs) are thought to be involved in photo-damage to the skin. MMP-1 is the major collagenolytic enzyme responsible for collagen destruction in skin tissue. To develop new anti-photoaging agents, a series of 2,2′-dithiocinnamate derivatives and 2,2′-dithio or 2-thiobenzoate derivatives were designed and synthesized. The biological activities of the synthesized compounds were assayed for ABTS [2,2′-azinobis-(3-ethyl-benzo- thiazoline-6-sulfonic acid)] radical scavenging activity, MMP-1 inhibitory activity, and cytotoxicity to human dermal fibroblast cells. Compounds with potential of resistance to UV irradiation were identified. These compounds are expected to be useful for preventing photo-damage to the skin.

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