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(S)-(+)-COP-OAC CATALYST, 95% is a chemical compound that serves as a catalyst in various organic synthesis reactions. It is a chiral source of copper(II) and is highly effective in promoting asymmetric cyclopropanation reactions. This catalyst is frequently utilized in the preparation of small-molecule compounds with specific stereochemistries. With a high purity level of 95%, it is considered a reliable and efficient reagent for synthetic chemistry applications, particularly in the development of pharmaceuticals and agrochemicals.

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  • 222400-03-5 Structure
  • Basic information

    1. Product Name: (S)-(+)-COP-OAC CATALYST, 95%
    2. Synonyms: [bis[μ-(acetato-κo: κo')]dipalladium]bis[1,1',1'',1'''-(η4-1,3-cyclobutadiene-1,2,3,4-tetrayl)tetrakis[benzene]]bis[μ-[(1-η:1,2,3,4,5-η)-2-[(4s)-4,5-dihydro-4-(1-methylethyl)-2-oxazolyl-κn3]-2,4-cyclo;[Bis[μ-(acetato-KO: KO')]dipalladium]bis[1,1',1'',1'''-(η:4-1,3-cyclobutadiene-1,2,3,4-tetrayl)tetrakis[benzene]]bis[μ-[(1-η::1,2,3,4,5-η:)-2-[(4S)-4,5-dihydro-4-(1-methylethyl)-2-oxazolyl-KN3]-2,4-cyclopentadien-1-ylidene]]dicobalt, Di-μ-acetatobis[η:5-(S)-(pR)-2-(2μ-(4μ-methylethyl)oxazolinyl)cyclopentadienyl,1-C,3μ-N)(η:4-tetraphenylcyclobutadiene)cobalt]dipalladium
    3. CAS NO:222400-03-5
    4. Molecular Formula: 2C28H20.2C11H14NO.2C2H3O2Pd.2Co
    5. Molecular Weight: 1514.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 222400-03-5.mol
  • Chemical Properties

    1. Melting Point: 250-257 °C (dec.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-(+)-COP-OAC CATALYST, 95%(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(+)-COP-OAC CATALYST, 95%(222400-03-5)
    11. EPA Substance Registry System: (S)-(+)-COP-OAC CATALYST, 95%(222400-03-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 222400-03-5(Hazardous Substances Data)

222400-03-5 Usage

Uses

Used in Pharmaceutical Industry:
(S)-(+)-COP-OAC CATALYST, 95% is used as a catalyst for the synthesis of small-molecule compounds with specific stereochemistries, which are crucial for the development of new pharmaceuticals. Its ability to promote asymmetric cyclopropanation reactions allows for the creation of chiral molecules that can have different biological activities and properties.
Used in Agrochemical Industry:
(S)-(+)-COP-OAC CATALYST, 95% is also used as a catalyst in the synthesis of small-molecule compounds with specific stereochemistries for the development of agrochemicals. These compounds can be used as active ingredients in pesticides, herbicides, and other agricultural products, contributing to increased crop yields and protection against pests.
Used in Organic Synthesis Research:
(S)-(+)-COP-OAC CATALYST, 95% is used as a research tool in organic synthesis, particularly for studying asymmetric cyclopropanation reactions. Its high purity and efficiency make it an ideal choice for exploring new reaction pathways and developing novel synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 222400-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,4,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 222400-03:
(8*2)+(7*2)+(6*2)+(5*4)+(4*0)+(3*0)+(2*0)+(1*3)=65
65 % 10 = 5
So 222400-03-5 is a valid CAS Registry Number.

222400-03-5 Well-known Company Product Price

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  • Aldrich

  • (661716)  (S)-(+)-COP-OAcCatalyst  95%

  • 222400-03-5

  • 661716-250MG

  • 5,312.97CNY

  • Detail
  • Aldrich

  • (661716)  (S)-(+)-COP-OAcCatalyst  95%

  • 222400-03-5

  • 661716-1G

  • 15,291.90CNY

  • Detail

222400-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,cobalt,(4S)-2-cyclopentyl-4-isopropyl-4,5-dihydrooxaz ole,palladium,(2,3,4-triphenylcyclobutyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:222400-03-5 SDS

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