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AKOS B028939, also known as 2-Buten-1-ol, is a colorless liquid chemical compound with the molecular formula C4H8O, characterized by a sharp, fruity odor. It is widely utilized across various industries as a solvent, intermediate, and fragrance ingredient, and serves as a precursor in the production of pharmaceuticals, pesticides, and plastics.

24581-99-5

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24581-99-5 Usage

Uses

Used in Pharmaceutical Industry:
AKOS B028939 is used as a precursor for the synthesis of various pharmaceutical compounds, contributing to the development of new medications and therapeutic agents.
Used in Pesticide Industry:
In the pesticide sector, AKOS B028939 is employed as a starting material for the production of different types of pesticides, aiding in the creation of effective solutions for pest control.
Used in Plastics Industry:
AKOS B028939 is utilized as a monomer or intermediate in the manufacturing process of various types of plastics, enhancing the versatility and applicability of plastic materials.
Used in Food and Beverage Industry:
AKOS B028939 is used as a flavoring agent, adding unique taste profiles to a range of food and beverage products, enhancing consumer appeal and product variety.
Used in Cosmetic and Personal Care Industry:
In the cosmetic and personal care sector, AKOS B028939 is employed as a fragrance ingredient, contributing to the creation of scents and aromas in products such as perfumes, lotions, and shampoos.
Used in Cleaning Products:
AKOS B028939 is used as a solvent in the formulation of cleaning products, improving their effectiveness in removing dirt and stains.
Used in Laboratory Processes:
In laboratory settings, AKOS B028939 is utilized as a solvent for various chemical reactions and processes, facilitating research and development activities.
It is crucial to adhere to proper safety measures when handling AKOS B028939 due to its flammable and potentially hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 24581-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24581-99:
(7*2)+(6*4)+(5*5)+(4*8)+(3*1)+(2*9)+(1*9)=125
125 % 10 = 5
So 24581-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9BrO4/c1-14-10(13)6-15-9-3-2-8(11)4-7(9)5-12/h2-5H,6H2,1H3

24581-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (4-bromo-2-formylphenoxy)acetate

1.2 Other means of identification

Product number -
Other names (4-bromo-2-formylphenoxy)acetic acid methyl ester

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:24581-99-5 SDS

24581-99-5Relevant academic research and scientific papers

Use of conformationally restricted benzamidines as arginine surrogates in the design of platelet GPIIb-IIIa receptor antagonists

Sall, Daniel J.,Arfsten, Ann E.,Bastian, Jolie A.,Denney, Michael L.,Harms, Cathy S.,McCowan, Jefferson R.,Morin Jr., John M.,Rose, Jack W.,Scarborough, Robert M.,Smyth, Mark S.,Um, Suzane L.,Utterback, Barbara G.,Vasileff, Robert T.,Wikel, James H.,Wyss, Virginia L.,Jakubowski, Joseph A.

, p. 2843 - 2857 (2007/10/03)

The use of 5,6-bicyclic amidines as arginine surrogates in the design of a novel class of potent platelet glycoprotein IIb-IIIa receptor (GPIIb-IIIa) antagonists is described. The additional conformational restriction offered by the bicyclic nucleus results in 20-400-fold increases in potency compared to the freely flexible, acyclic benzamidine counterpart. The design, synthesis, structure-activity relationships (SAR), and in vitro activity of this novel class of GPIIb-IIIa antagonists are presented.

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