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1073630-49-5

(R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1073630-49-5 Structure

  • Basic information

    1. Product Name: (R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene
    2. Synonyms: (R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene
    3. CAS NO:1073630-49-5
    4. Molecular Formula:
    5. Molecular Weight: 366.619
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1073630-49-5.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: (R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene(1073630-49-5)
    11. EPA Substance Registry System: (R)-6-tert-butyldiphenylsilyloxy-2-methyl-2-heptene(1073630-49-5)

  • 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: 1073630-49-5(Hazardous Substances Data)

1073630-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073630-49-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,6,3 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1073630-49:
(9*1)+(8*0)+(7*7)+(6*3)+(5*6)+(4*3)+(3*0)+(2*4)+(1*9)=135
135 % 10 = 5
So 1073630-49-5 is a valid CAS Registry Number.

1073630-49-5Relevant articles and documents

A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: Application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide e

Chatterjee, Sucheta,Ghadigaonkar, Sneha,Sur, Payel,Sharma, Anubha,Chattopadhyay, Subrata

, p. 8067 - 8076 (2014)

The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols.

Novel, Acyclically Substituted Furopyrimidine Derivatives and Use Thereof

-

Page/Page column 33, (2009/12/28)

The present application relates to novel, acyclically substituted furopyrimidine derivatives, methods for their production, their use for the treatment and/or prophylaxis of diseases and their use for the production of medicinal products for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular diseases.

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