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39098-85-6

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39098-85-6 Usage

Description

3-Oxobutanoyl chloride, also known as acetylacetyl chloride, is a colorless liquid compound with a pungent odor. It is a versatile chemical that can undergo a variety of reactions, including esterification, acylation, and condensation, making it useful in the production of a wide range of compounds. It is often used as a reagent in organic synthesis and is a key intermediate in the production of pharmaceuticals, agrochemicals, and polymers. However, it is highly reactive and should be handled with care, as it can cause skin and eye irritation, and inhaling its vapors can be harmful. Overall, 3-Oxobutanoyl chloride is an important building block in the chemical industry due to its reactivity and versatility in organic synthesis.

Uses

Used in Pharmaceutical Industry:
3-Oxobutanoyl chloride is used as a key intermediate for the synthesis of various pharmaceuticals. Its reactivity and versatility in organic synthesis make it an important building block in the development of new drugs.
Used in Agrochemical Industry:
3-Oxobutanoyl chloride is used as a reagent in the synthesis of agrochemicals. Its ability to undergo various reactions allows for the production of a wide range of compounds used in agriculture.
Used in Polymer Industry:
3-Oxobutanoyl chloride is used as a monomer or intermediate in the production of polymers. Its reactivity and versatility in organic synthesis contribute to the development of new polymer materials with specific properties.
Used in Organic Synthesis:
3-Oxobutanoyl chloride is used as a reagent in organic synthesis for a variety of reactions, including esterification, acylation, and condensation. Its ability to participate in these reactions makes it a valuable tool in the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 39098-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39098-85:
(7*3)+(6*9)+(5*0)+(4*9)+(3*8)+(2*8)+(1*5)=156
156 % 10 = 6
So 39098-85-6 is a valid CAS Registry Number.

39098-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Oxobutanoyl chloride

1.2 Other means of identification

Product number -
Other names (acetoxy)acetyl chloride

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:39098-85-6 SDS

39098-85-6Upstream product

39098-85-6Relevant articles and documents

Sodium carbonate as a solid-phase reagent for the generation of acetylketene

Bell, Kelcey,Sadasivam, Dhandapani V.,Gudipati, Indra Reddy,Ji, Hua,Birney, David

, p. 1295 - 1297 (2009)

Reaction of a toluene solution of 3-oxobutanoyl chloride (14) with Na2CO3 in the presence of a catalytic amount of triethylamine at -78 °C generates a solution of acetylketene (2), the dimer of which was isolated. Acetylketene (2) was trapped with 2-propanone, 2-propanol, and ethyl vinyl ether.

6-Methyl-2H-1,3-oxazin-2,4(3H)dione-3-sulfohalides

-

, (2008/06/13)

3-Sulfohalides of 6-methyl-2H-1,3-oxazin-2,4(3H)-dione of the formula I STR1 in which X represents fluorine or chlorine are prepared by reacting fluorosulfonyl isocyanate or chlorosulfonyl isocyanate, at a temperature of from -35° to +70° C, optionally in the presence of an inert solvent, with diketene, acetoacetyl fluoride, acetoacetyl chloride, acetoacetic acid or an isopropenyl ester of the formula CH2 =C(OOCR)-CH3 in which R represents an alkyl radical having from 1 to 4 carbon atoms, a substituted or unsubstituted phenyl or benzyl radical.

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