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142074-96-2

(S)-(-)-1-(phenoxycarbonyl)-4-(4-chlorophenyl)-2-pyrroline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142074-96-2 Structure

  • Basic information

    1. Product Name: (S)-(-)-1-(phenoxycarbonyl)-4-(4-chlorophenyl)-2-pyrroline
    2. Synonyms:
    3. CAS NO:142074-96-2
    4. Molecular Formula:
    5. Molecular Weight: 299.757
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142074-96-2.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: (S)-(-)-1-(phenoxycarbonyl)-4-(4-chlorophenyl)-2-pyrroline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(-)-1-(phenoxycarbonyl)-4-(4-chlorophenyl)-2-pyrroline(142074-96-2)
    11. EPA Substance Registry System: (S)-(-)-1-(phenoxycarbonyl)-4-(4-chlorophenyl)-2-pyrroline(142074-96-2)

  • 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: 142074-96-2(Hazardous Substances Data)

142074-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142074-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,7 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142074-96:
(8*1)+(7*4)+(6*2)+(5*0)+(4*7)+(3*4)+(2*9)+(1*6)=112
112 % 10 = 2
So 142074-96-2 is a valid CAS Registry Number.

142074-96-2Downstream Products

142074-96-2Relevant articles and documents

Catalytic asymmetric arylation of N-substituted 2-pyrrolines with aryl triflates

Ozawa, Fumiyuki,Hayashi, Tamio

, p. 267 - 277 (2007/10/02)

Catalytic asymmetric arylation of 1-(alkoxycarbonyl)-2-pyrrolines (4) with aryl triflates (1) in benzene in the presence of a base and a palladium catalyst, prepared in situ by mixing Pd(OAc)2 and (R)-BINAP, gives optically active (R)-1-(alkoxycarbonyl)5-aryl-2-pyrrolines (5) of up to 83percent ee. together with the regioisomers 1-(alkoxycarbonyl)-5-aryl-3-pyrrolines (6).

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