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72521-05-2

2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72521-05-2 Structure

  • Basic information

    1. Product Name: 2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile
    2. Synonyms: 2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile
    3. CAS NO:72521-05-2
    4. Molecular Formula:
    5. Molecular Weight: 428.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72521-05-2.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: 2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile(72521-05-2)
    11. EPA Substance Registry System: 2-benzylamino-2-deoxy-3-O-(β-D-galactopyranosyl)-D-glucononitrile(72521-05-2)

  • 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: 72521-05-2(Hazardous Substances Data)

72521-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72521-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,2 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72521-05:
(7*7)+(6*2)+(5*5)+(4*2)+(3*1)+(2*0)+(1*5)=102
102 % 10 = 2
So 72521-05-2 is a valid CAS Registry Number.

72521-05-2Downstream Products

72521-05-2Relevant articles and documents

Large scale synthesis of linker-modified sialyl Lewis(X), Lewis(X) and N-acetyllactosamine

Kretzschmar, Gerhard,Stahl, Wilhelm

, p. 6341 - 6358 (2007/10/03)

The synthesis of sialyl-Lewis(X) (1b), Lewis(X) (2) and N- acetyllactosamine (3), each being attached to the 1β-O-(6-amino)hexyl handle, were scaled up to gram amounts to obtain sufficient material for thorough pharmaceutical evaluations and for derivatisations aiming at more potent selectin antagonists. The disaccharide 3 was synthesised from inexpensive lactose to provide a versatile building block, either to be used for alternative approaches to the Lewis type oligosaccharides, or to prepare polyvalent LacNAc templates to be further elaborated by glycosyltransferase reactions. All syntheses were directed to reasonable large scale procedures, especially by minimising the number of steps and the use of heavy metal salts in glycosylations.

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