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CAS

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1206768-23-1

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

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  • 1206768-23-1 Structure

  • Basic information

    1. Product Name: (S)-1-(4-bromophenyl)-2-phenylpropan-1-one
    2. Synonyms: (S)-1-(4-bromophenyl)-2-phenylpropan-1-one
    3. CAS NO:1206768-23-1
    4. Molecular Formula:
    5. Molecular Weight: 289.172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206768-23-1.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-(4-bromophenyl)-2-phenylpropan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-(4-bromophenyl)-2-phenylpropan-1-one(1206768-23-1)
    11. EPA Substance Registry System: (S)-1-(4-bromophenyl)-2-phenylpropan-1-one(1206768-23-1)

  • 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: 1206768-23-1(Hazardous Substances Data)

1206768-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206768-23-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,7,6 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1206768-23:
(9*1)+(8*2)+(7*0)+(6*6)+(5*7)+(4*6)+(3*8)+(2*2)+(1*3)=151
151 % 10 = 1
So 1206768-23-1 is a valid CAS Registry Number.

1206768-23-1Downstream Products

1206768-23-1Relevant articles and documents

Catalytic Asymmetric Formal Insertion of Aryldiazoalkanes into the C-H Bond of Aldehydes: Synthesis of Enantioenriched Acyclic α-Tertiary Aryl Ketones

Kang, Byung Chul,Nam, Dong Guk,Hwang, Geum-Sook,Ryu, Do Hyun

, p. 4810 - 4813 (2015)

A novel, catalytic enantioselective route to synthesize a variety of α-tertiary aryl ketones via a boron Lewis acid promoted formal insertion of aryldiazoalkane into the C-H bond of both aromatic and aliphatic aldehydes is described. In the presence of ch

SYNTHESIZING METHOD OF α-TERTIARY ARYL KETONE

-

Paragraph 0081; 0082; 0084; 0085; 0086, (2017/08/02)

The present invention relates to a synthesizing method of alpha-tertiary aryl ketone. The synthesizing method of alpha-tertiary aryl ketone synthesizes alpha-tertiary aryl ketone by making aldehyde react with aryldiazoalkanes under a chiral boron Lewis ac

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