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288852-06-2

methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 288852-06-2 Structure

  • Basic information

    1. Product Name: methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate
    2. Synonyms: methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate
    3. CAS NO:288852-06-2
    4. Molecular Formula:
    5. Molecular Weight: 373.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 288852-06-2.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: methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate(288852-06-2)
    11. EPA Substance Registry System: methyl (S)-3-(4-methoxyphenyl)methoxy-2-(N-phenylmethoxycarbonyl)aminopropanoate(288852-06-2)

  • 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: 288852-06-2(Hazardous Substances Data)

288852-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288852-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,8,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 288852-06:
(8*2)+(7*8)+(6*8)+(5*8)+(4*5)+(3*2)+(2*0)+(1*6)=192
192 % 10 = 2
So 288852-06-2 is a valid CAS Registry Number.

288852-06-2Relevant articles and documents

Synthesis of a six-carbon sialic acid using an indium-mediated coupling.

Chappell,Halcomb

, p. 2003 - 2005 (2000)

[reaction: see text] The synthesis of a six-carbon truncated sialic acid is described. A key step in the synthesis was an indium-mediated allyl addition to a serine-derived aldehyde. Careful choice of protecting groups was found to be necessary in order to prevent unwanted side reactions throughout the sequence. The truncated sialic acid was obtained in a form suitable for activation as a glycosyl donor.

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