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(2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609286-43-2 Structure
  • Basic information

    1. Product Name: (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate
    2. Synonyms: (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate
    3. CAS NO:1609286-43-2
    4. Molecular Formula:
    5. Molecular Weight: 415.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609286-43-2.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: (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate(1609286-43-2)
    11. EPA Substance Registry System: (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-methoxybenzyloxy)-3-phenylpropanoate(1609286-43-2)
  • 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: 1609286-43-2(Hazardous Substances Data)

1609286-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609286-43-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,2,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609286-43:
(9*1)+(8*6)+(7*0)+(6*9)+(5*2)+(4*8)+(3*6)+(2*4)+(1*3)=182
182 % 10 = 2
So 1609286-43-2 is a valid CAS Registry Number.

1609286-43-2Relevant articles and documents

CHIRAL FLUORINATING REAGENTS

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, (2014/05/24)

This invention relates to fluorinating agents and, more particularly, to chiral non-racemic fluorinating agents useful for enantioselective fluorination, as well as to their synthesis and use and other subject matter. The fluorinating agents are based on a substituted 1,4-diazabicyclo[2.2.2]octane (DABCO) skeleton and provide electrophillic fluorine enantioselectively.

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