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851909-12-1

methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]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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  • 851909-12-1 Structure

  • Basic information

    1. Product Name: methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate
    2. Synonyms: methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate
    3. CAS NO:851909-12-1
    4. Molecular Formula:
    5. Molecular Weight: 279.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851909-12-1.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 (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate(851909-12-1)
    11. EPA Substance Registry System: methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate(851909-12-1)

  • 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: 851909-12-1(Hazardous Substances Data)

851909-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851909-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 851909-12:
(8*8)+(7*5)+(6*1)+(5*9)+(4*0)+(3*9)+(2*1)+(1*2)=181
181 % 10 = 1
So 851909-12-1 is a valid CAS Registry Number.

851909-12-1Relevant articles and documents

Systematic study of the synthesis of macrocyclic dipeptide β-turn mimics possessing 8-, 9-, and 10- membered rings by ring-closing metathesis

Kaul, Ramesh,Surprenant, Simon,Lubell, William D.

, p. 3838 - 3844 (2005)

A systematic study was performed to establish general synthesis protocols for forming enantiomerically pure macrocyclic dipeptide lactams. Focusing on macrocycles of 8-, 9-, and 10-membered rings, effective syntheses were achieved by a sequence featuring

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