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1011309-59-3

2-amino-2-methyl-6-heptenoic acid amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1011309-59-3 Structure

  • Basic information

    1. Product Name: 2-amino-2-methyl-6-heptenoic acid amide
    2. Synonyms: 2-amino-2-methyl-6-heptenoic acid amide
    3. CAS NO:1011309-59-3
    4. Molecular Formula:
    5. Molecular Weight: 156.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1011309-59-3.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: 2-amino-2-methyl-6-heptenoic acid amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-2-methyl-6-heptenoic acid amide(1011309-59-3)
    11. EPA Substance Registry System: 2-amino-2-methyl-6-heptenoic acid amide(1011309-59-3)

  • 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: 1011309-59-3(Hazardous Substances Data)

1011309-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1011309-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,3,0 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1011309-59:
(9*1)+(8*0)+(7*1)+(6*1)+(5*3)+(4*0)+(3*9)+(2*5)+(1*9)=83
83 % 10 = 3
So 1011309-59-3 is a valid CAS Registry Number.

1011309-59-3Upstream product

1011309-59-3Relevant articles and documents

A cross-metathesis route to functionalized α-methyl α-substituted amino acids

Storcken, Roy P. M.,Panella, Lavinia,Van Delft, Floris L.,Kaptein, Bernard,Broxterman, Quirinus B.,Schoemaker, Hans E.,Rutjes, Floris P. J. T.

, p. 161 - 164 (2007)

A chemoenzymatic approach to the synthesis of functionalized α-methyl α-substituted amino acids is detailed. This involves amidasemediated enzymatic resolution of α-methyl α-substituted side-chain ω-unsaturated amino acids followed by functionalization via cross-metathesis.

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