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930608-35-8

C11H16Cl3NO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 930608-35-8 Structure

  • Basic information

    1. Product Name: C11H16Cl3NO
    2. Synonyms: C11H16Cl3NO
    3. CAS NO:930608-35-8
    4. Molecular Formula:
    5. Molecular Weight: 284.613
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 930608-35-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C11H16Cl3NO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H16Cl3NO(930608-35-8)
    11. EPA Substance Registry System: C11H16Cl3NO(930608-35-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 930608-35-8(Hazardous Substances Data)

930608-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 930608-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,0,6,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 930608-35:
(8*9)+(7*3)+(6*0)+(5*6)+(4*0)+(3*8)+(2*3)+(1*5)=158
158 % 10 = 8
So 930608-35-8 is a valid CAS Registry Number.

930608-35-8Downstream Products

930608-35-8Relevant articles and documents

Catalytic asymmetric synthesis of chiral allylic esters

Cannon, Jeffrey S.,Kirsch, Stefan F.,Overman, Larry E.

supporting information; experimental part, p. 15185 - 15191 (2010/12/25)

A broadly useful catalytic enantioselective synthesis of branched allylic esters from prochiral (Z)-2-alkene-1-ols has been developed. The starting allylic alcohol is converted to its trichloroacetimidate intermediate by reaction with trichloroacetonitrile, either in situ or in a separate step, and this intermediate undergoes clean enantioselective SN2′ substitution with a variety of carboxylic acids in the presence of the palladium(II) catalyst (Rp,S)-di-μ-acetatobis[(η5- 2-(2′-(4′-methylethyl)oxazolinyl)cyclopentadienyl-1-C,3′-N) (η4-tetraphenylcyclobutadiene)cobalt]dipalladium, (R p,S)-[COP-OAc]2, or its enantiomer. The scope and limitations of this useful catalytic asymmetric allylic esterification are defined.

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