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CAS

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1156540-85-0

(1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1156540-85-0 Structure

  • Basic information

    1. Product Name: (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide
    2. Synonyms: (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide
    3. CAS NO:1156540-85-0
    4. Molecular Formula:
    5. Molecular Weight: 245.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1156540-85-0.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: (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide(1156540-85-0)
    11. EPA Substance Registry System: (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide(1156540-85-0)

  • 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: 1156540-85-0(Hazardous Substances Data)

1156540-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1156540-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,6,5,4 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1156540-85:
(9*1)+(8*1)+(7*5)+(6*6)+(5*5)+(4*4)+(3*0)+(2*8)+(1*5)=150
150 % 10 = 0
So 1156540-85-0 is a valid CAS Registry Number.

1156540-85-0Downstream Products

1156540-85-0Relevant articles and documents

Asymmetric Co(II)-catalyzed cyclopropanation with succinimidyl diazoacetate: General synthesis of chiral cyclopropyl carboxamides

Ruppel, Joshua V.,Gauthier, Ted J.,Snyder, Nicole L.,Perman, Jason A.,Zhang, X. Peter

, p. 2273 - 2276 (2009)

[Co(P1)] is an effective catalyst for asymmetric cyclopropanation with succinimidyl diazoacetate. The Co(II)-catalyzed reaction is suitable for various olefins, providing the desired cyclopropane succinimidyl esters in high yields and excellent diastereo-

ASYMMETRIC CYCLOPROPANATION WITH SUCCINIMIDYL DIAZOACETATE

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Page/Page column 45-46; 49; 58-59, (2010/09/03)

Cobalt(ll) complexes of the D2-symmetric chiral porphyrins are effective catalysts for asymmetric cyclopropanation reactions with succinimidyl diazoacetate. The Co-catalyzed reaction is suitable for various olefins, providing the corresponding cyclopropane succinimidyl esters in high yields and excellent diastereo- and enantio-selectivity. The resulting enantioenriched cyclopropane succinimidyl esters can serve as convenient synthons for the general synthesis of optically active cyclopropyl carboxamides through mild reactions with a wide range of amine derivatives, including unprotected peptides and amino sugars

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