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475291-71-5

methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 475291-71-5 Structure

  • Basic information

    1. Product Name: methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate
    2. Synonyms: methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate
    3. CAS NO:475291-71-5
    4. Molecular Formula:
    5. Molecular Weight: 317.385
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 475291-71-5.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: methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate(475291-71-5)
    11. EPA Substance Registry System: methyl (2R,3R)-2-allyl-3-[(benzyloxy)carbonylamino]hex-5-enoate(475291-71-5)

  • 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: 475291-71-5(Hazardous Substances Data)

475291-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475291-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,2,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 475291-71:
(8*4)+(7*7)+(6*5)+(5*2)+(4*9)+(3*1)+(2*7)+(1*1)=175
175 % 10 = 5
So 475291-71-5 is a valid CAS Registry Number.

475291-71-5Relevant articles and documents

Synthesis of Cyclic β-Amino Acid Esters from Methionine, Allylglycine, and Serine

Gardiner, James,Anderson, Kelly H.,Downard, Alison,Abell, Andrew D.

, p. 3375 - 3382 (2007/10/03)

Here we report a versatile ring-closing metathesis-based approach to 5-, 6-, and 7-membered cyclic β-amino esters starting with simple and readily available building blocks-methionine, allylglycine, and serine-where the nature of the amino acid determines

Synthesis of substituted cyclohexenyl-based β-amino acids by ring-closing metathesis

Abell, Andrew D.,Gardiner, James

, p. 3663 - 3666 (2007/10/03)

(equation presented) A versatile ring-closing metathesis (RCM) approach has been developed for the preparation of cis and trans cyclohexenyl-based β-amino acids that are either unsubstituted (3) or substituted (10 and 12) at the α-position.

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