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345306-16-3

(S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 345306-16-3 Structure

  • Basic information

    1. Product Name: (S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one
    2. Synonyms: (S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one
    3. CAS NO:345306-16-3
    4. Molecular Formula:
    5. Molecular Weight: 316.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 345306-16-3.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: (S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one(345306-16-3)
    11. EPA Substance Registry System: (S)-3-Methyl-6-nonyl-6-phenyl-tetrahydro-pyran-2-one(345306-16-3)

  • 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: 345306-16-3(Hazardous Substances Data)

345306-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 345306-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,5,3,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 345306-16:
(8*3)+(7*4)+(6*5)+(5*3)+(4*0)+(3*6)+(2*1)+(1*6)=123
123 % 10 = 3
So 345306-16-3 is a valid CAS Registry Number.

345306-16-3Downstream Products

345306-16-3Relevant articles and documents

Efficient 1,8- and 1,9-asymmetric inductions in the Grignard reaction of δ- and ε-keto esters of 1,1′-binaphthalen-2-ols with an oligoether tether as the 2′-substituent: Application to the synthesis of (-)-malyngolide

Date,Tamai,Hattori,Takayama,Kamikubo,Miyano

, p. 645 - 653 (2007/10/03)

Efficient 1,8- and 1,9-asymmetric inductions in the Grignard reaction of podand-type δ- (3,4) and ε-keto esters (5,6) are achieved in the presence of MgBr2·OEt2 with up to 97 and 82% optical yields, respectively, by using 2′-[3-(2-methoxyethoxy)propoxy]-1,1′-binaphthalen-2-ol as the chiral auxiliary. The 1,8-asymmetric inductive Grignard reaction has been advantageously utilized in the key step of a synthesis of (-)-malyngolide.

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