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Ethyl diacetoacetate is an organic compound that serves as an important intermediate in the synthesis of various chemical compounds. It is characterized by its ability to participate in a wide range of chemical reactions, making it a versatile building block in the field of organic chemistry.

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  • 603-69-0 Structure
  • Basic information

    1. Product Name: Ethyl diacetoacetate
    2. Synonyms: Acetoacetic acid, 2-acetyl-, ethyl ester;Butanoic acid, 2-acetyl-3-oxo-, ethyl ester;Ethyl 2-acetyl-3-oxobutanoate;Ethyl 2-acetylacetoacetate;DIACETOACETIC ACID ETHYL ESTER;ETHYL 2-ACETYL-3-OXOBUTYRATE;ETHYL DIACETOACETATE;ETHYL DIACETYL ACETATE
    3. CAS NO:603-69-0
    4. Molecular Formula: C8H12O4
    5. Molecular Weight: 172.18
    6. EINECS: 210-053-3
    7. Product Categories: Pharmaceutical Intermediates;Acetics acid and esters;C8 to C9;Carbonyl Compounds;Esters
    8. Mol File: 603-69-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 104-105 °C17 mm Hg(lit.)
    3. Flash Point: 185 °F
    4. Appearance: clear colorless to yellow liquid
    5. Density: 1.104 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 8.24E-06mmHg at 25°C
    7. Refractive Index: n20/D 1.47(lit.)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 6.93±0.46(Predicted)
    11. Water Solubility: Not miscible in water.
    12. BRN: 775014
    13. CAS DataBase Reference: Ethyl diacetoacetate(CAS DataBase Reference)
    14. NIST Chemistry Reference: Ethyl diacetoacetate(603-69-0)
    15. EPA Substance Registry System: Ethyl diacetoacetate(603-69-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39-37/39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 603-69-0(Hazardous Substances Data)

603-69-0 Usage

Uses

Used in Organic Synthesis:
Ethyl diacetoacetate is used as a key intermediate for the synthesis of various organic compounds. Its reactivity and functional groups allow it to be easily modified and incorporated into more complex molecules, facilitating the creation of a diverse array of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl diacetoacetate is used as a starting material for the production of various drugs and pharmaceutical agents. Its ability to be readily transformed into other compounds makes it a valuable component in the development of new medications and therapies.
Used in Agrochemicals:
Ethyl diacetoacetate is also utilized in the agrochemical sector, where it serves as a precursor for the synthesis of various agrochemical products. Its involvement in the production of these compounds contributes to the development of effective solutions for agricultural applications.
Used in Dye Industry:
In the dye industry, Ethyl diacetoacetate is employed in the preparation of specific dyes, such as 3-acetyl-6-chloro-7-hydroxy-4-methylcoumarin. Its role in the synthesis of these dyes highlights its versatility and importance in the production of colorants for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 603-69-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 603-69:
(5*6)+(4*0)+(3*3)+(2*6)+(1*9)=60
60 % 10 = 0
So 603-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O4/c1-4-12-8(11)7(5(2)9)6(3)10/h11H,4H2,1-3H3

603-69-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (B20149)  Ethyl diacetoacetate, 97%   

  • 603-69-0

  • 10g

  • 834.0CNY

  • Detail
  • Alfa Aesar

  • (B20149)  Ethyl diacetoacetate, 97%   

  • 603-69-0

  • 50g

  • 2000.0CNY

  • Detail
  • Alfa Aesar

  • (B20149)  Ethyl diacetoacetate, 97%   

  • 603-69-0

  • 250g

  • 8010.0CNY

  • Detail

603-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl diacetoacetate

1.2 Other means of identification

Product number -
Other names Ethyl 2-acetyl-3-oxobutanoate

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:603-69-0 SDS

603-69-0Relevant articles and documents

Synthesis and cyclization reaction of pyrazolin-5-one derivatives

Jung, Jae-Chul,Blake Watkins,Avery, Mitchell A.

, p. 77 - 94 (2007/10/03)

A versatile synthetic method for preparing 3-pyrazolin-5-ones and 5,8-dihydro-1H-pyrazolo[1,2-a]pyridazines from simple β-keto esters is demonstrated. The synthetic strategies involve the acylation of β-keto esters, cyclocondensation with hydrazine followed by trapping with a diene under oxidative conditions.

Method for preparing chiral diphosphines

-

, (2008/06/13)

The invention concerns a method for preparing a compound of formula (1) wherein: A represents naphthyl or phenyl optionally substituted; and Ar1, Ar2independently represent a saturated or aromatic carbocyclic group, optionally substituted.

Asymmetric hydrogenation method of a ketonic compound and derivative

-

, (2008/06/13)

The present invention relates to a process for the asymmetric hydrogenation of a ketonic compound and derivative. The invention relates to the use of optically active metal complexes as catalysts for the asymmetric hydrogenation of a ketonic compound and derivative. The process for the asymmetric hydrogenation of a ketonic compound and derivative is characterized in that the asymmetric hydrogenation of said compound is carried out in the presence of an effective amount of a metal complex comprising as ligand an optically active diphosphine corresponding to one of the following formulae: STR1

Acetylation of β-diketone copper(II) chelates by treatment with ketene

Matare,Bohac,Hrnciar

, p. 381 - 382 (2007/10/02)

A new efficient method for preparation of acyclic α-acetylated β-diketone copper(II) chelates and their corresponding geminal triketones by treatment of starting β-diketone cuprates 1 with ketene is described.

Cycloaliphatic unsaturated ketones as fragrance modifying agents

-

, (2008/06/13)

New cycloaliphatic unsaturated ketones and their use as perfuming and odor-modifying agents in the manufacture of perfumes and perfumed products, and as flavoring and taste-modifying agents in the preparation of foodstuffs in general and imitation flavors for foodstuffs, beverages, animal feeds, pharmaceutical preparations and tobacco products. Methods for preparing the said new compounds and certain of the starting materials used for their synthesis.

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