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Allyl chlorooxoacetate, with the molecular formula C4H5ClO3, is a colorless liquid chemical compound that serves as a versatile building block in organic synthesis. As an ester formed from the reaction between an alcohol and an organic or inorganic acid, it is known for its strong, pungent odor and is classified as a hazardous chemical. Its reactivity and ability to form new bonds make it a valuable precursor in the production of pharmaceuticals, agrochemicals, and other organic compounds.

74503-07-4

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74503-07-4 Usage

Uses

Used in Pharmaceutical Industry:
Allyl chlorooxoacetate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form new bonds and facilitate the creation of complex molecular structures.
Used in Agrochemical Industry:
In the agrochemical sector, allyl chlorooxoacetate is utilized as a precursor in the development of pesticides and other agrochemicals, contributing to the production of effective and targeted crop protection agents.
Used in Organic Synthesis:
As a versatile compound in organic chemistry, allyl chlorooxoacetate is used as a reagent in the synthesis of a wide range of organic compounds, including specialty chemicals and intermediates for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 74503-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74503-07:
(7*7)+(6*4)+(5*5)+(4*0)+(3*3)+(2*0)+(1*7)=114
114 % 10 = 4
So 74503-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClO3/c1-2-3-9-5(8)4(6)7/h2H,1,3H2

74503-07-4 Well-known Company Product Price

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  • Aldrich

  • (738875)  Allyl oxalyl chloride  97%

  • 74503-07-4

  • 738875-1G

  • 293.67CNY

  • Detail
  • Aldrich

  • (738875)  Allyl oxalyl chloride  97%

  • 74503-07-4

  • 738875-5G

  • 969.93CNY

  • Detail

74503-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl 2-chloro-2-oxoacetate

1.2 Other means of identification

Product number -
Other names allyloxyoxalyl 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:74503-07-4 SDS

74503-07-4Downstream Products

74503-07-4Relevant academic research and scientific papers

Synthesis and application of oxalic acid monoester derivatives

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Paragraph 0015-0018, (2020/12/08)

The invention relates to synthesis and application of oxalic acid monoester-containing compounds as shown in a general formula (I) which is described in the specification. The compounds represent a broad-spectrum efficient insecticidal and bactericidal agent structure type. The oxalic acid monoester-containing compounds can well control aphids, plutella xylostella and spodoptera exigua when used as novel insecticidal bactericides; the compounds can also be used for preventing and treating cucumber brown blotch, cucumber bacterial angular leaf spot, cucumber fusarium wilt, cucumber downy mildew, cucumber powdery mildew, tomato bacterial leaf spot and rice sheath blight. R in the general formula (I) is as defined in the specification.

Design, synthesis and insecticidal activities of novel N-oxalyl derivatives of neonicotinoid compound

Zhao, Yu,Wang, Gang,Li, Yongqiang,Wang, Suhua,Li, Zhengming

experimental part, p. 475 - 479 (2010/10/20)

Ten novel neonicotinoid derivatives containing N-oxalyl groups were designed and synthesized, and their structures were characterized by 1H NMR, MS, IR, elemental analysis and single crystal X-ray diffraction analysis. The insecticidal activities of the new compounds were evaluated. The results of bioassays indicated that some of these title compounds exhibited excellent insecticidal activities.

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