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(-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374647-50-3 Structure
  • Basic information

    1. Product Name: (-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene
    2. Synonyms: (-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene
    3. CAS NO:1374647-50-3
    4. Molecular Formula:
    5. Molecular Weight: 246.393
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374647-50-3.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: (-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene(1374647-50-3)
    11. EPA Substance Registry System: (-)-1-methoxy-2-(3-methylnon-1-en-3-yl)benzene(1374647-50-3)
  • 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: 1374647-50-3(Hazardous Substances Data)

1374647-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374647-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,6,4 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1374647-50:
(9*1)+(8*3)+(7*7)+(6*4)+(5*6)+(4*4)+(3*7)+(2*5)+(1*0)=183
183 % 10 = 3
So 1374647-50-3 is a valid CAS Registry Number.

1374647-50-3Downstream Products

1374647-50-3Relevant articles and documents

Enantioselective synthesis of all-carbon quaternary stereogenic centers via copper-catalyzed asymmetric allylic alkylation of (Z)-allyl bromides with organolithium reagents

Faans-Mastral, Martn,Vitale, Romina,Prez, Manuel,Feringa, Ben L.

supporting information, p. 4209 - 4212 (2015/03/14)

A copper/phosphoramidite catalyzed asymmetric allylic alkylation of Z trisubstituted allyl bromides with organolithium reagents is reported. The reaction affords all-carbon quaternary stereogenic centers in high yields and very good regio- and enantiosele

Enantioselective synthesis of tertiary and quaternary stereogenic centers: Copper/phosphoramidite-catalyzed allylic alkylation with organolithium reagents

Fananas-Mastral, Martin,Perez, Manuel,Bos, Pieter H.,Rudolph, Alena,Harutyunyan, Syuzanna R.,Feringa, Ben L.

supporting information; experimental part, p. 1922 - 1925 (2012/04/17)

An efficient and highly enantioselective copper-catalyzed allylic alkylation of disubstituted allyl halides with primary and secondary organolithium reagents using phosphoramidite ligands is reported. The use of trisubstituted allyl bromides allows, for the first time, the enantioselective synthesis of all-carbon quaternary stereogenic centers with these reactive organometallic reagents.

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