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CAS

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934021-52-0

(2S,3S)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 934021-52-0 Structure

  • Basic information

    1. Product Name: (2S,3S)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol
    2. Synonyms: (2S,3S)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol
    3. CAS NO:934021-52-0
    4. Molecular Formula:
    5. Molecular Weight: 388.507
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 934021-52-0.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)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol(934021-52-0)
    11. EPA Substance Registry System: (2S,3S)-1,4-bis[(2-hydroxyethyl)(benzyl)amino]butane-2,3-diol(934021-52-0)

  • 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: 934021-52-0(Hazardous Substances Data)

934021-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 934021-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,0,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 934021-52:
(8*9)+(7*3)+(6*4)+(5*0)+(4*2)+(3*1)+(2*5)+(1*2)=140
140 % 10 = 0
So 934021-52-0 is a valid CAS Registry Number.

934021-52-0Relevant articles and documents

Synthesis of (2S,2′S)-bimorpholine N,N′-quaternary salts as chiral phase transfer catalysts

Lippur, Kristin,Kanger, Tonis,Kriis, Kadri,Kailas, Tiiu,Mueuerisepp, Aleksander-Mati,Pehk, Tonis,Lopp, Margus

, p. 137 - 141 (2007)

(2S,2′S)-Bimorpholine was synthesized starting from (R,R)-tartaric acid ester acetal in six steps in 50% of the total yield. Key steps include: cyanide catalyzed amidation and one-step cyclization with p-toluenesulfonyl imidazole. Derivatization of N,N′-d

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