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862895-53-2

(S)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 862895-53-2 Structure

  • Basic information

    1. Product Name: (S)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide
    2. Synonyms: (S)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide
    3. CAS NO:862895-53-2
    4. Molecular Formula:
    5. Molecular Weight: 328.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 862895-53-2.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)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide(862895-53-2)
    11. EPA Substance Registry System: (S)-2-(2-bromophenyl)-N-(1-hydroxy-3-methylbutan-2-yl)-2-methylpropanamide(862895-53-2)

  • 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: 862895-53-2(Hazardous Substances Data)

862895-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862895-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,8,9 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 862895-53:
(8*8)+(7*6)+(6*2)+(5*8)+(4*9)+(3*5)+(2*5)+(1*3)=222
222 % 10 = 2
So 862895-53-2 is a valid CAS Registry Number.

862895-53-2Relevant articles and documents

A dramatic switch of enantioselectivity in asymmetric heck reaction by benzylic substituents of ligands

Wu, Wen-Qiong,Peng, Qian,Dong, Da-Xuan,Hou, Xue-Long,Wu, Yun-Dong

experimental part, p. 9717 - 9725 (2009/02/04)

A series of benzylic substituted P,N-ligands 1 and 2 have been synthesized. The Pd-complexes of these ligands show high catalytic activity and enantioselectivity in catalyzing the asymmetric Heck reaction. A dramatic switch in enantioselectivity is realized using ligands with and without substituents at the benzylic position of the ligand. Ligands 1 with H as the substituents offer products in (R)-configuration while ligands 2 with the methyl as substituents result in (S)-configuration products. In most cases high enantioselectivities are achieved. Density functional theory calculations on the reaction mechanism as well as X-ray analysis of 1a-PdCl2 and 2a-PdCl2 complexes provide a rational explanation for the above observations.

A highly efficient palladacycle catalyst for hydrophenylation of C-, N-, and O-substituted bicyclic alkenes under aerobic condition

Yuan, Ke,Zhang, Ting Ke,Hou, Xue Long

, p. 6085 - 6088 (2007/10/03)

A new phosphine-free palladacycle catalyst 4 was prepared from benzyl oxazoline in high yield and fully characterized. With it as catalyst, hydrophenylation reactions of a wide range of bicyclic alkenes, not only norbomene and norborriadiene but also oxa-

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