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tert-butyl (2S,3S,4S)-4-(methoxycarbonyl)-3,4-bis(benzyloxy)-1-hydroxybutan-2-ylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1253734-93-8 Structure
  • Basic information

    1. Product Name: tert-butyl (2S,3S,4S)-4-(methoxycarbonyl)-3,4-bis(benzyloxy)-1-hydroxybutan-2-ylcarbamate
    2. Synonyms:
    3. CAS NO:1253734-93-8
    4. Molecular Formula:
    5. Molecular Weight: 459.54
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1253734-93-8.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: tert-butyl (2S,3S,4S)-4-(methoxycarbonyl)-3,4-bis(benzyloxy)-1-hydroxybutan-2-ylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (2S,3S,4S)-4-(methoxycarbonyl)-3,4-bis(benzyloxy)-1-hydroxybutan-2-ylcarbamate(1253734-93-8)
    11. EPA Substance Registry System: tert-butyl (2S,3S,4S)-4-(methoxycarbonyl)-3,4-bis(benzyloxy)-1-hydroxybutan-2-ylcarbamate(1253734-93-8)
  • 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: 1253734-93-8(Hazardous Substances Data)

1253734-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1253734-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,7,3 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1253734-93:
(9*1)+(8*2)+(7*5)+(6*3)+(5*7)+(4*3)+(3*4)+(2*9)+(1*3)=158
158 % 10 = 8
So 1253734-93-8 is a valid CAS Registry Number.

1253734-93-8Downstream Products

1253734-93-8Relevant articles and documents

A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate

Passiniemi, Mikko,Koskinen, Ari M.P.

, p. 2816 - 2822 (2010)

Asymmetric synthesis of the title compound was accomplished starting from l-serine. Stannoxane-mediated lactamization provided the key intermediate in good yield. Georg Thieme Verlag Stuttgart.

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